Variant report

Variant	rs7615206
Chromosome Location	chr3:49937505-49937506
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:110)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:110 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:49937360-49937510	GM12878	blood:	n/a	n/a
2	CTCF	chr3:49937420-49937570	MCF-7	breast:	n/a	n/a
3	CTCF	chr3:49937341-49937581	A549	lung:	n/a	n/a
4	CTCF	chr3:49937350-49937538	GM19240	blood:	n/a	n/a
5	CTCF	chr3:49937380-49937530	GM12871	blood:	n/a	n/a
6	CTCF	chr3:49937440-49937590	A549	lung:	n/a	n/a
7	CTCF	chr3:49937360-49937510	GM12870	blood:	n/a	n/a
8	CTCF	chr3:49937440-49937590	HCT-116	colon:	n/a	n/a
9	RAD21	chr3:49937221-49937634	H1-hESC	embryonic stem cell:	n/a	n/a
10	RAD21	chr3:49937358-49937542	A549	lung:	n/a	n/a
11	CTCF	chr3:49937380-49937530	HEK293	kidney:	n/a	n/a
12	CTCF	chr3:49937248-49937600	K562	blood:	n/a	n/a
13	CTCF	chr3:49937367-49937530	Gliobla	brain:	n/a	n/a
14	CTCF	chr3:49937400-49937550	GM06990	blood:	n/a	n/a
15	CTCF	chr3:49937378-49937521	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:49937400-49937550	GM12865	blood:	n/a	n/a
17	CTCF	chr3:49937351-49937535	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr3:49937279-49937548	HepG2	liver:	n/a	n/a
19	CTCF	chr3:49937380-49937530	HMEC	breast:	n/a	n/a
20	CTCF	chr3:49937360-49937510	RPTEC	kidney:	n/a	n/a
21	SMARCC1	chr3:49937415-49938985	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr3:49937360-49937510	GM12875	blood:	n/a	n/a
23	CTCF	chr3:49937406-49937526	GM10248	blood:	n/a	n/a
24	CTCF	chr3:49937380-49937530	GM12864	blood:	n/a	n/a
25	RAD21	chr3:49937295-49937505	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr3:49937386-49937534	GM10266	blood:	n/a	n/a
27	CTCF	chr3:49937360-49937510	HCM	heart:	n/a	n/a
28	CTCF	chr3:49937332-49937556	GM12891	blood:	n/a	n/a
29	CTCF	chr3:49937382-49937505	GM19239	blood:	n/a	n/a
30	CTCF	chr3:49937329-49937546	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr3:49937360-49937510	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr3:49937285-49937574	GM12878	blood:	n/a	n/a
33	CTCF	chr3:49937325-49937548	K562	blood:	n/a	n/a
34	CTCF	chr3:49937323-49937579	Medullo	brain:	n/a	n/a
35	CTCF	chr3:49937440-49937590	HMEC	breast:	n/a	n/a
36	CTCF	chr3:49937347-49937533	HepG2	liver:	n/a	n/a
37	CTCF	chr3:49937221-49937634	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:49937397-49937506	Fibrobl	skin:	n/a	n/a
39	CTCF	chr3:49937360-49937510	AG09319	gingival:	n/a	n/a
40	CTCF	chr3:49937380-49937530	AG09309	skin:	n/a	n/a
41	TFAP2C	chr3:49937474-49938632	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr3:49937360-49937510	GM12871	blood:	n/a	n/a
43	CTCF	chr3:49937360-49937510	HMF	breast:	n/a	n/a
44	RAD21	chr3:49937213-49937838	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr3:49937219-49937624	K562	blood:	n/a	n/a
46	CTCF	chr3:49937227-49937638	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr3:49937309-49937575	NHEK	skin:	n/a	n/a
48	CTCF	chr3:49937400-49937550	HRE	kidney:	n/a	n/a
49	CTCF	chr3:49937440-49937590	HEEpiC	esophagus:	n/a	n/a
50	RAD21	chr3:49937229-49937586	HepG2	liver:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49935827..49937610-chr3:49975872..49978554,2	K562	blood:
2	chr3:49933351..49938041-chr3:49938966..49942332,9	K562	blood:
3	chr3:49904537..49906285-chr3:49936889..49938764,2	K562	blood:
4	chr3:49839049..49842350-chr3:49936029..49940414,4	K562	blood:
5	chr3:49823044..49824946-chr3:49937035..49939087,2	MCF-7	breast:
6	chr3:49934674..49936736-chr3:49937436..49939317,2	K562	blood:
7	chr3:49927426..49930206-chr3:49934919..49938158,3	K562	blood:
8	chr3:49838968..49841390-chr3:49937411..49939491,2	MCF-7	breast:
9	chr3:49932972..49936126-chr3:49936946..49940007,3	MCF-7	breast:
10	chr3:49878485..49879205-chr3:49936998..49938153,4	MCF-7	breast:
11	chr3:49840382..49843169-chr3:49936309..49938239,3	K562	blood:

No data

Variant related genes	Relation type
MST1R	TF binding region
ENSG00000228008	TF binding region
ENSG00000230698	Chromatin interaction
ENSG00000004534	Chromatin interaction
ENSG00000228008	Chromatin interaction
ENSG00000164078	Chromatin interaction
ENSG00000176095	Chromatin interaction
ENSG00000185614	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs10049087	0.81[JPT][hapmap]
rs1062633	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs10865959	0.86[CHB][hapmap]
rs11130222	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11130228	0.81[JPT][hapmap]
rs11130233	0.89[JPT][hapmap]
rs11706185	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11709503	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11709573	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11712056	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11714324	0.95[ASN][1000 genomes]
rs11721204	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12496973	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs12634780	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13060128	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs13071931	0.86[LWK][hapmap];1.00[YRI][hapmap]
rs13077403	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13079006	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13082703	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1317140	0.89[CHB][hapmap]
rs17304079	0.86[LWK][hapmap];1.00[YRI][hapmap]
rs17657664	0.94[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17657688	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1799843	0.89[CHB][hapmap]
rs1799845	0.89[CHB][hapmap]
rs2013208	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2230590	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240326	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240327	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240328	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2240329	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2247510	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap]
rs2252833	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2276864	0.86[CHB][hapmap]
rs2280406	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2352969	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2352975	0.89[CHB][hapmap]
rs2352984	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2353579	0.82[JPT][hapmap]
rs2526747	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[ASN][1000 genomes]
rs2526748	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2526751	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2526754	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2624815	0.80[ASN][1000 genomes]
rs2624819	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2624821	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2624822	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2624832	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2624834	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2624843	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2624853	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2681776	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2681779	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2681780	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2681781	0.89[CHD][hapmap];0.82[JPT][hapmap]
rs2777888	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2883057	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2883059	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34034116	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34312088	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34654589	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35275715	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36022378	0.87[ASN][1000 genomes]
rs3733134	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3774733	0.82[JPT][hapmap]
rs3774734	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs3774759	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3796386	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4688688	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4688689	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688690	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688753	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4688754	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4688755	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688758	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs55692411	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62262114	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6446193	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6446195	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6762477	1.00[ASW][hapmap];0.87[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.80[ASN][1000 genomes]
rs6765484	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6771546	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6772095	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6774354	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6785500	0.81[YRI][hapmap]
rs6792892	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6793528	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs7061	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs7430334	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[ASN][1000 genomes]
rs7613360	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7613875	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7615318	0.91[LWK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs7621026	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7621352	0.82[JPT][hapmap]
rs7626952	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7627864	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7627910	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7628058	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7629936	0.89[CHB][hapmap]
rs7634441	0.80[ASN][1000 genomes]
rs7635601	0.85[LWK][hapmap];1.00[YRI][hapmap]
rs7648174	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs868891	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9311446	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs952594	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9682295	0.80[ASN][1000 genomes]
rs9814664	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs9821675	0.90[JPT][hapmap]
rs9861216	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs9866695	0.90[CHD][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1796352	chr3:49687101-49949959	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription 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	90 gene(s)	inside rSNPs	diseases
2	nsv834688	chr3:49811115-50019299	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv876766	chr3:49817450-49961780	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh 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	47 gene(s)	inside rSNPs	diseases
4	nsv876767	chr3:49918751-50153356	Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs7615206	RBM6	cis	Whole Blood	GTEx
rs7615206	RBM6	cis	cerebellum	SCAN
rs7615206	RBM6	cis	parietal	SCAN
rs7615206	QRICH1	cis	cerebellum	SCAN
rs7615206	RBM6	cis	lung	GTEx
rs7615206	RBM6	cis	Thyroid	GTEx
rs7615206	RNF123	cis	cerebellum	SCAN
rs7615206	RBM6	Cis_1M	lymphoblastoid	RTeQTL
rs7615206	RBM6	cis	Artery Aorta	GTEx
rs7615206	RBM6	cis	Artery Tibial	GTEx
rs7615206	RBM6	cis	Skin Sun Exposed Lower leg	GTEx
rs7615206	RNF123	cis	parietal	SCAN
rs7615206	ARIH2	cis	cerebellum	SCAN
rs7615206	RBM6	cis	Esophagus Mucosa	GTEx
rs7615206	RBM6	cis	Esophagus Muscularis	GTEx
rs7615206	RBM6	cis	Adipose Subcutaneous	GTEx
rs7615206	RBM6	cis	Heart Left Ventricle	GTEx
rs7615206	RBM6	cis	Nerve Tibial	GTEx
rs7615206	CELSR3	cis	parietal	SCAN

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49919600-49937800	Weak transcription	Small Intestine	intestine
2	chr3:49920000-49943000	Weak transcription	Brain Anterior Caudate	brain
3	chr3:49920200-49938400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr3:49920400-49938200	Weak transcription	Left Ventricle	heart
5	chr3:49920600-49938200	Weak transcription	Fetal Muscle Leg	muscle
6	chr3:49920600-49938200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:49924000-49937600	Strong transcription	Fetal Stomach	stomach
8	chr3:49924600-49937600	Weak transcription	K562	blood
9	chr3:49924800-49938200	Weak transcription	Right Ventricle	heart
10	chr3:49925200-49941200	Weak transcription	Brain Germinal Matrix	brain
11	chr3:49926600-49938400	Weak transcription	Aorta	Aorta
12	chr3:49927000-49938000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:49927400-49937600	Weak transcription	Placenta	Placenta
14	chr3:49927600-49940400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:49928600-49943000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr3:49929000-49938400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr3:49929600-49941200	Weak transcription	Ovary	ovary
18	chr3:49931400-49938400	Weak transcription	Colon Smooth Muscle	Colon
19	chr3:49931400-49943600	Weak transcription	Brain Hippocampus Middle	brain
20	chr3:49933200-49938200	Weak transcription	Adipose Nuclei	Adipose
21	chr3:49933400-49939600	Weak transcription	Fetal Brain Female	brain
22	chr3:49933800-49941400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr3:49934200-49938600	Weak transcription	Fetal Lung	lung
24	chr3:49934400-49941400	Weak transcription	Brain Angular Gyrus	brain
25	chr3:49935200-49937600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr3:49935400-49937800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr3:49935400-49940000	Weak transcription	Spleen	Spleen
28	chr3:49935800-49937600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr3:49936000-49937600	Enhancers	HMEC	breast
30	chr3:49936000-49939000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:49936200-49938800	Transcr. at gene 5' and 3'	NHEK	skin
32	chr3:49936200-49939000	Enhancers	Lung	lung
33	chr3:49936200-49941000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:49936400-49937600	Genic enhancers	Fetal Intestine Small	intestine
35	chr3:49936400-49940800	Enhancers	Pancreas	Pancrea
36	chr3:49936600-49937800	Enhancers	Gastric	stomach
37	chr3:49936800-49937600	Enhancers	Fetal Intestine Large	intestine
38	chr3:49936800-49937600	Enhancers	A549	lung
39	chr3:49936800-49937800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:49936800-49939600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:49937000-49940800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr3:49937200-49938000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:49937200-49938000	Flanking Active TSS	Stomach Mucosa	stomach
44	chr3:49937200-49938000	Flanking Active TSS	Hela-S3	cervix
45	chr3:49937400-49937600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr3:49937400-49937800	Flanking Active TSS	Colonic Mucosa	Colon
47	chr3:49937400-49938000	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr3:49937400-49938000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr3:49937400-49938000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
50	chr3:49937400-49938200	Enhancers	Esophagus	oesophagus

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