Variant report

Variant	rs12350740
Chromosome Location	chr9:139637541-139637542
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:139637460-139637610	GM12874	blood:	n/a	n/a
2	CTCF	chr9:139637480-139637630	HFF-Myc	foreskin:	n/a	n/a
3	GABPA	chr9:139637012-139637584	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr9:139637427-139637645	Fibrobl	skin:	n/a	n/a
5	CTCF	chr9:139637460-139637610	MCF-7	breast:	n/a	n/a
6	SIN3A	chr9:139637206-139637612	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr9:139637480-139637630	GM12869	blood:	n/a	n/a
8	CTCF	chr9:139637466-139637579	LNCaP	prostate:	n/a	n/a
9	RAD21	chr9:139637394-139637624	HepG2	liver:	n/a	n/a
10	CTBP2	chr9:139637236-139637740	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:139637480-139637630	HL-60	blood:	n/a	n/a
12	CTCF	chr9:139637420-139637570	GM12872	blood:	n/a	n/a
13	CTCF	chr9:139637438-139637659	Gliobla	brain:	n/a	n/a
14	CTCF	chr9:139637430-139637643	A549	lung:	n/a	n/a
15	ZBTB7A	chr9:139637382-139637655	HepG2	liver:	n/a	n/a
16	CTCF	chr9:139637460-139637610	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr9:139637431-139637630	K562	blood:	n/a	n/a
18	CTCF	chr9:139637422-139637664	GM12892	blood:	n/a	n/a
19	CTCF	chr9:139637458-139637603	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:139637465-139637642	GM13977	blood:	n/a	n/a
21	CTCF	chr9:139637440-139637590	AG04450	lung:	n/a	n/a
22	ZBTB7A	chr9:139637177-139637695	ECC-1	luminal epithelium:	n/a	n/a
23	CTCF	chr9:139637460-139637610	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr9:139637440-139637590	BE2_C	brain:	n/a	n/a
25	CTCF	chr9:139637460-139637610	HEK293	kidney:	n/a	n/a
26	CTCF	chr9:139637460-139637610	GM12868	blood:	n/a	n/a
27	ZNF143	chr9:139637252-139637677	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:139637446-139637617	GM12878	blood:	n/a	n/a
29	CTCF	chr9:139637420-139637570	AG09309	skin:	n/a	n/a
30	CTCF	chr9:139637480-139637630	K562	blood:	n/a	n/a
31	CTCF	chr9:139637449-139637617	IMR90	lung:	n/a	n/a
32	CTCF	chr9:139637480-139637630	HCT-116	colon:	n/a	n/a
33	CTCF	chr9:139637472-139637619	ProgFib	skin:	n/a	n/a
34	CTCF	chr9:139637420-139637570	HCM	heart:	n/a	n/a
35	CTCF	chr9:139637520-139637670	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr9:139637460-139637610	HMEC	breast:	n/a	n/a
37	CTCF	chr9:139637460-139637610	RPTEC	kidney:	n/a	n/a
38	CTCF	chr9:139637369-139637609	A549	lung:	n/a	n/a
39	CTCF	chr9:139637520-139637670	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr9:139637440-139637590	GM12870	blood:	n/a	n/a
41	CTCF	chr9:139637500-139637650	GM12871	blood:	n/a	n/a
42	CTCF	chr9:139637442-139637627	MCF-7	breast:	n/a	n/a
43	ZBTB7A	chr9:139637430-139637631	HepG2	liver:	n/a	n/a
44	CTCF	chr9:139637460-139637610	HCT-116	colon:	n/a	n/a
45	ZBTB7A	chr9:139637351-139637655	K562	blood:	n/a	n/a
46	CTCF	chr9:139637460-139637610	BE2_C	brain:	n/a	n/a
47	CTCF	chr9:139637483-139637680	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr9:139637460-139637610	HVMF	connective:	n/a	n/a
49	CTCF	chr9:139637457-139637617	MCF-7	breast:	n/a	n/a
50	RAD21	chr9:139637417-139637645	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:139637526-139637576	SK-N-SH_RA	brain:	n/a
2	chr9:139637526-139637576	HRE	kidney:	n/a
3	chr9:139637526-139637576	H1-hESC	embryonic stem cell:	embryo
4	chr9:139637526-139637576	A549	lung:	n/a
5	chr9:139637526-139637576	Hepatocyte	liver:	n/a
6	chr9:139637526-139637576	MCF10A-Er-Src	breast:	n/a
7	chr9:139637526-139637576	HCM	heart:	n/a
8	chr9:139637526-139637576	NB4	blood:	n/a
9	chr9:139637526-139637576	BJ	skin:	n/a
10	chr9:139637526-139637576	Hela-S3	cervix:	n/a
11	chr9:139637526-139637576	GM12891	blood:	n/a
12	chr9:139637526-139637576	PrEC	prostate:	n/a
13	chr9:139637526-139637576	HEEpiC	esophagus:	n/a
14	chr9:139637526-139637576	HepG2	liver:	n/a
15	chr9:139637526-139637576	HCF	heart:	n/a
16	chr9:139637526-139637576	ovcar-3	ovarian:	n/a
17	chr9:139637526-139637576	HRPEpiC	eye:	n/a
18	chr9:139637526-139637576	AG04450	lung:	fetal
19	chr9:139637526-139637576	MCF-7	breast:	n/a
20	chr9:139637526-139637576	AoSMC	blood vessel:	n/a
21	chr9:139637526-139637576	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:139637526-139637576	HCT-116	colon:	n/a
23	chr9:139637526-139637576	CMK	blood:	n/a
24	chr9:139637526-139637576	AG09319	gingival:	n/a
25	chr9:139637526-139637576	ProgFib	skin:	n/a
26	chr9:139637526-139637576	GM12892	blood:	n/a
27	chr9:139637526-139637576	NT2-D1	testis:	n/a
28	chr9:139637526-139637576	AG09309	skin:	n/a
29	chr9:139637526-139637576	HAEpiC	amniotic membrane:	n/a
30	chr9:139637526-139637576	SKMC	muscle:	n/a
31	chr9:139637526-139637576	BE2_C	brain:	n/a
32	chr9:139637526-139637576	NHDF-neo	bronchial:	n/a
33	chr9:139637526-139637576	AG04449	skin:	fetal
34	chr9:139637526-139637576	T-47D	breast:	n/a
35	chr9:139637526-139637576	GM06990	blood:	n/a
36	chr9:139637526-139637576	HL-60	blood:	n/a
37	chr9:139637526-139637576	HRCEpiC	kidney:	n/a
38	chr9:139637526-139637576	HEK293	kidney:	embryo
39	chr9:139637526-139637576	LNCaP	prostate:	n/a
40	chr9:139637526-139637576	GM19239	blood:	n/a
41	chr9:139637526-139637576	NH-A	brain:	n/a
42	chr9:139637526-139637576	RPTEC	kidney:	n/a
43	chr9:139637526-139637576	HUVEC	blood vessel:	n/a
44	chr9:139637526-139637576	PFSK-1	brain:	n/a
45	chr9:139637526-139637576	IMR90	lung:	fetal
46	chr9:139637526-139637576	Caco-2	colon:	n/a
47	chr9:139637526-139637576	HIPEpiC	eye:	n/a
48	chr9:139637526-139637576	AG10803	skin:	n/a
49	chr9:139637526-139637576	U87	brain:	n/a
50	chr9:139637526-139637576	HMEC	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:139620067..139623891-chr9:139635001..139639921,9	MCF-7	breast:
2	chr9:139637504..139640391-chr9:139641154..139643856,2	MCF-7	breast:
3	chr9:139610819..139629219-chr9:139630372..139645615,53	MCF-7	breast:
4	chr9:139635847..139638838-chr9:139639718..139641868,2	K562	blood:
5	chr9:139635253..139638024-chr9:139639450..139641983,3	MCF-7	breast:
6	chr9:139569086..139572014-chr9:139637166..139639125,2	MCF-7	breast:

No data

Variant related genes	Relation type
LCN10	TF binding region
LCN10	CpG island
ENSG00000204003	Chromatin interaction
ENSG00000267206	Chromatin interaction
ENSG00000165716	Chromatin interaction
ENSG00000233016	Chromatin interaction
ENSG00000169692	Chromatin interaction

Extended variants
information (count: 125 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10114790	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10114897	0.89[AMR][1000 genomes]
rs10118376	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10118736	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10283881	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10747034	0.83[ASN][1000 genomes]
rs10747035	0.83[ASN][1000 genomes]
rs10870117	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10870118	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10870120	0.85[ASN][1000 genomes]
rs1108607	0.88[ASN][1000 genomes]
rs11145852	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11145853	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11145854	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11145857	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11145862	0.91[ASN][1000 genomes]
rs11145867	0.85[ASN][1000 genomes]
rs12004931	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12342911	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12345308	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12684980	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13294615	0.85[ASN][1000 genomes]
rs1360879	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1360880	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1360881	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2282258	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2282259	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2282261	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2484659	0.89[ASN][1000 genomes]
rs2484660	0.89[ASN][1000 genomes]
rs2784067	0.87[ASN][1000 genomes]
rs2784068	0.87[ASN][1000 genomes]
rs2784071	0.94[ASN][1000 genomes]
rs2811727	0.96[ASN][1000 genomes]
rs2811728	0.93[ASN][1000 genomes]
rs2811730	0.89[ASN][1000 genomes]
rs2811732	0.88[ASN][1000 genomes]
rs2811735	0.87[ASN][1000 genomes]
rs28678356	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35852083	0.87[ASN][1000 genomes]
rs4419903	0.85[ASN][1000 genomes]
rs4585841	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4880133	0.81[ASN][1000 genomes]
rs4880135	0.81[ASN][1000 genomes]
rs62582222	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6560646	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67957838	0.80[ASN][1000 genomes]
rs7041329	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7041806	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7042091	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7045311	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7045416	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7848644	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7848807	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7859350	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7859621	0.88[ASN][1000 genomes]
rs7862031	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs879467	0.88[ASN][1000 genomes]
rs9411219	0.81[ASN][1000 genomes]
rs9411221	0.83[ASN][1000 genomes]
rs9411224	0.90[ASN][1000 genomes]
rs9411225	0.93[ASN][1000 genomes]
rs9411269	0.81[ASN][1000 genomes]
rs9411272	0.87[ASN][1000 genomes]
rs945379	0.94[ASN][1000 genomes]
rs9886752	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1849811	chr9:138939662-139755001	Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
2	esv1822553	chr9:138967205-139755539	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
3	nsv894326	chr9:139057463-139647074	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	260 gene(s)	inside rSNPs	diseases
4	nsv894337	chr9:139069713-139669111	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	261 gene(s)	inside rSNPs	diseases
5	esv1851120	chr9:139101947-139711758	Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	275 gene(s)	inside rSNPs	diseases
6	nsv430118	chr9:139101947-139795504	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	299 gene(s)	inside rSNPs	diseases
7	nsv894351	chr9:139124856-139679387	Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	262 gene(s)	inside rSNPs	diseases
8	nsv540342	chr9:139218422-139973312	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	317 gene(s)	inside rSNPs	diseases
9	esv2758204	chr9:139252829-139826485	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
10	esv2759720	chr9:139252829-139826485	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
11	nsv469918	chr9:139254317-140068342	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
12	esv1836722	chr9:139301583-139669111	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
13	esv1799492	chr9:139341612-139711758	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
14	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
15	esv1803718	chr9:139368953-139643023	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
16	esv1851291	chr9:139371234-139669111	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	200 gene(s)	inside rSNPs	diseases
17	nsv894385	chr9:139376426-139647074	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	199 gene(s)	inside rSNPs	diseases
18	nsv894386	chr9:139376426-139693992	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	208 gene(s)	inside rSNPs	diseases
19	nsv1039149	chr9:139376829-139991102	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	303 gene(s)	inside rSNPs	diseases
20	esv1820573	chr9:139377938-139643023	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
21	esv1839109	chr9:139377938-139660589	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
22	esv1829857	chr9:139385438-139760041	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
23	esv1819204	chr9:139388365-139758238	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
24	esv1803407	chr9:139393591-139643023	Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
25	esv1803979	chr9:139395473-139979276	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
26	esv1831778	chr9:139395473-139979276	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
27	esv1821575	chr9:139395473-140068342	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
28	nsv8579	chr9:139399884-139654708	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
29	nsv894392	chr9:139403102-139669111	Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
30	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
31	nsv894409	chr9:139483954-139860264	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	209 gene(s)	inside rSNPs	diseases
32	esv1846227	chr9:139487092-139643023	Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
33	esv1794085	chr9:139487092-139649379	Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
34	esv1837438	chr9:139487092-139660589	Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
35	nsv894421	chr9:139487092-139669111	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
36	nsv894422	chr9:139487092-139776400	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
37	nsv894428	chr9:139496028-139647074	ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
38	nsv894431	chr9:139522101-139642961	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
39	nsv894432	chr9:139522101-139869914	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	205 gene(s)	inside rSNPs	diseases
40	nsv894440	chr9:139544437-139841512	Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
41	nsv894441	chr9:139544437-139860264	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
42	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
43	nsv540348	chr9:139550414-139687876	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
44	nsv894445	chr9:139556771-139669111	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
45	nsv1043160	chr9:139560991-139665208	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
46	nsv540349	chr9:139560991-139665208	Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
47	nsv894448	chr9:139598108-139660589	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
48	nsv894449	chr9:139598108-139669111	Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
49	nsv894450	chr9:139598108-139776400	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	130 gene(s)	inside rSNPs	diseases
50	nsv894451	chr9:139598108-139995065	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs12350740	LCN8	cis	Whole Blood	GTEx
rs12350740	LCN8	Cis_1M	lymphoblastoid	RTeQTL
rs12350740	LCN8	cis	Stomach	GTEx
rs12350740	LCN8	cis	lung	GTEx
rs12350740	LCN8	cis	Muscle Skeletal	GTEx

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139634800-139638000	Enhancers	Fetal Heart	heart
2	chr9:139635000-139637800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
3	chr9:139635200-139638000	Bivalent Enhancer	Placenta	Placenta
4	chr9:139635200-139638000	Enhancers	Pancreas	Pancrea
5	chr9:139635200-139638200	Enhancers	Gastric	stomach
6	chr9:139635400-139637600	Bivalent Enhancer	Fetal Stomach	stomach
7	chr9:139635400-139637600	Enhancers	Lung	lung
8	chr9:139635400-139637600	Flanking Bivalent TSS/Enh	HepG2	liver
9	chr9:139635400-139637800	Bivalent Enhancer	Stomach Mucosa	stomach
10	chr9:139635600-139637800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:139635600-139638000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr9:139635600-139638400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:139636000-139637800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
14	chr9:139636000-139638000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:139636200-139637600	Enhancers	Primary hematopoietic stem cells	blood
16	chr9:139636200-139640600	Active TSS	Left Ventricle	heart
17	chr9:139636400-139637600	Bivalent Enhancer	GM12878-XiMat	blood
18	chr9:139636400-139637800	Bivalent Enhancer	Colonic Mucosa	Colon
19	chr9:139636400-139639800	Weak transcription	K562	blood
20	chr9:139636600-139637600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:139636600-139639200	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr9:139636600-139641200	Enhancers	Spleen	Spleen
23	chr9:139636800-139637600	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr9:139637000-139637600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr9:139637000-139637600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr9:139637000-139637600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr9:139637000-139637600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr9:139637000-139637600	Bivalent Enhancer	Esophagus	oesophagus
29	chr9:139637000-139637800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr9:139637000-139638000	Enhancers	Primary B cells from cord blood	blood
31	chr9:139637000-139638200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:139637000-139639200	Weak transcription	Right Atrium	heart
33	chr9:139637200-139637600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr9:139637200-139637600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:139637200-139637600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
36	chr9:139637200-139637800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr9:139637200-139637800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr9:139637200-139638400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr9:139637400-139637600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:139637400-139637600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:139637400-139637600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr9:139637400-139637600	Enhancers	Liver	Liver
43	chr9:139637400-139637600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
44	chr9:139637400-139637800	Bivalent Enhancer	Adipose Nuclei	Adipose
45	chr9:139637400-139637800	Bivalent Enhancer	Fetal Intestine Large	intestine
46	chr9:139637400-139637800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr9:139637400-139637800	Enhancers	Fetal Thymus	thymus
48	chr9:139637400-139638600	Enhancers	Right Ventricle	heart
49	chr9:139637400-139639600	Enhancers	Primary B cells from peripheral blood	blood

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