Variant report

Variant	rs941653
Chromosome Location	chr14:35592538-35592539
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYBL2	chr14:35590302-35592745	HepG2	liver:	n/a	n/a
2	POLR2A	chr14:35590240-35592733	MCF10A-Er-Src	breast:	n/a	n/a
3	MAX	chr14:35590517-35593028	HepG2	liver:	n/a	chr14:35591490-35591509 chr14:35591494-35591505 chr14:35591495-35591504 chr14:35591493-35591506 chr14:35591495-35591504 chr14:35591495-35591504 chr14:35591486-35591502
4	GATA3	chr14:35592366-35592582	SH-SY5Y	brain:	n/a	n/a
5	CHD2	chr14:35592475-35592586	HepG2	liver:	n/a	n/a
6	E2F4	chr14:35592511-35592566	GM12878	blood:	n/a	n/a
7	MBD4	chr14:35590468-35593050	HepG2	liver:	n/a	n/a
8	UBTF	chr14:35592508-35592572	K562	blood:	n/a	n/a
9	MAZ	chr14:35590587-35592764	IMR90	lung:	n/a	chr14:35591490-35591509 chr14:35591494-35591505 chr14:35591495-35591504 chr14:35591493-35591506 chr14:35591495-35591504 chr14:35591495-35591504 chr14:35591486-35591502
10	MXI1	chr14:35590835-35592578	HepG2	liver:	n/a	chr14:35591496-35591505
11	TEAD4	chr14:35590503-35592888	HepG2	liver:	n/a	chr14:35590965-35590974
12	POLR2A	chr14:35590105-35592819	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA2	chr14:35592264-35592699	SH-SY5Y	brain:	n/a	n/a
14	MYC	chr14:35590760-35592721	MCF10A-Er-Src	breast:	n/a	chr14:35591490-35591509 chr14:35591494-35591505 chr14:35591495-35591504 chr14:35591493-35591506 chr14:35591495-35591504 chr14:35591495-35591504 chr14:35591486-35591502
15	GATA3	chr14:35592324-35592784	T-47D	breast:	n/a	n/a
16	SPI1	chr14:35592460-35592945	HL-60	blood:	n/a	n/a
17	RUNX3	chr14:35590657-35592779	GM12878	blood:	n/a	chr14:35591947-35591956 chr14:35591947-35591956 chr14:35592205-35592220
18	SIN3AK20	chr14:35590267-35592753	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:35592400-35592550	AG04449	skin:	n/a	n/a
20	MYBL2	chr14:35590348-35592882	HepG2	liver:	n/a	n/a
21	WRNIP1	chr14:35590954-35592751	GM12878	blood:	n/a	n/a
22	HEY1	chr14:35590628-35592545	HepG2	liver:	n/a	chr14:35591728-35591743
23	SIN3AK20	chr14:35590585-35592778	MCF-7	breast:	n/a	n/a
24	ZNF384	chr14:35592358-35592580	K562	blood:	n/a	chr14:35592404-35592412
25	HCFC1	chr14:35589880-35593328	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr14:35590768-35592723	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:35592496-35592553	HUVEC	blood vessel:	n/a	n/a
28	RCOR1	chr14:35590826-35592637	K562	blood:	n/a	n/a
29	CREB1	chr14:35590396-35592761	HepG2	liver:	n/a	n/a
30	POLR2A	chr14:35592493-35592564	ProgFib	skin:	n/a	n/a
31	NFIC	chr14:35590663-35592762	HepG2	liver:	n/a	n/a
32	ELF1	chr14:35590710-35592625	HepG2	liver:	n/a	chr14:35591675-35591684
33	MAX	chr14:35590707-35592625	MCF-7	breast:	n/a	chr14:35591490-35591509 chr14:35591494-35591505 chr14:35591495-35591504 chr14:35591493-35591506 chr14:35591495-35591504 chr14:35591495-35591504 chr14:35591486-35591502

No.	Distal block	Cell Line	Cell type
1	chr14:35450245..35452169-chr14:35590215..35593362,3	MCF-7	breast:
2	chr14:35341168..35344675-chr14:35590606..35593872,6	MCF-7	breast:
3	chr14:35591775..35593424-chr14:35873275..35875126,2	K562	blood:
4	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
5	chr14:35568810..35572401-chr14:35587846..35592624,4	MCF-7	breast:
6	chr14:35591658..35595888-chr14:35872338..35875561,5	K562	blood:
7	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
8	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
9	chr14:35589196..35594400-chr14:35871301..35877730,13	MCF-7	breast:
10	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
11	chr14:35589240..35593864-chr14:35869008..35876501,20	MCF-7	breast:
12	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
13	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
14	chr14:35341498..35344850-chr14:35591184..35593267,3	K562	blood:
15	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:

Variant related genes	Relation type
PPP2R3C	TF binding region
ENSG00000258704	Chromatin interaction
ENSG00000259090	Chromatin interaction
ENSG00000258738	Chromatin interaction
ENSG00000151327	Chromatin interaction
ENSG00000100883	Chromatin interaction
ENSG00000100906	Chromatin interaction
ENSG00000198604	Chromatin interaction

Extended variants
information (count: 106 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1028449	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1048990	0.92[CEU][hapmap]
rs1056879	0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs11156875	1.00[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.86[YRI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11851907	0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs12587376	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12589079	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12589278	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs12881698	0.81[ASN][1000 genomes]
rs12887779	0.81[AMR][1000 genomes]
rs12892552	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12895051	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs17102967	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs17102970	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs17103005	0.83[JPT][hapmap]
rs17103034	0.81[ASN][1000 genomes]
rs17103104	0.92[CEU][hapmap]
rs17103120	0.92[CEU][hapmap]
rs17113838	0.91[CEU][hapmap]
rs1712349	0.86[JPT][hapmap]
rs1967723	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2010648	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2038255	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2143950	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2179890	0.82[JPT][hapmap]
rs2236167	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs2273158	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2383689	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2415260	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2415261	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2415262	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28365850	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28399702	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28765972	0.83[ASN][1000 genomes]
rs2899830	0.84[ASN][1000 genomes]
rs34286037	0.84[AMR][1000 genomes]
rs35030792	0.81[ASN][1000 genomes]
rs3809449	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4594164	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5014384	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56027918	0.83[ASN][1000 genomes]
rs57075379	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57725522	0.81[AMR][1000 genomes]
rs60693825	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61125355	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61136372	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62625038	0.86[ASN][1000 genomes]
rs71421921	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7142489	0.82[JPT][hapmap]
rs7144423	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7144617	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7145474	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7145883	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7149177	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7153068	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7153331	0.80[ASN][1000 genomes]
rs7153550	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7153626	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7154306	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7155696	0.81[ASN][1000 genomes]
rs7156322	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7158416	0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs7158634	0.82[ASN][1000 genomes]
rs7159324	0.92[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.86[YRI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7160160	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72664807	0.81[ASN][1000 genomes]
rs8006884	0.81[ASN][1000 genomes]
rs8007274	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8009093	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8013540	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8014091	0.81[ASN][1000 genomes]
rs8014377	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8015622	0.81[ASN][1000 genomes]
rs8017225	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs8018114	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs8019179	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs8019351	0.82[ASN][1000 genomes]
rs932473	0.86[JPT][hapmap]
rs9671773	0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS 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 target site	73 gene(s)	inside rSNPs	diseases
2	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	nsv564264	chr14:35482797-35732369	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv901615	chr14:35485748-35630175	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv870305	chr14:35488290-35852349	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv1052800	chr14:35509858-35607117	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv1044515	chr14:35510785-35756317	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv564265	chr14:35512335-35624831	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv1046992	chr14:35527239-35724227	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv1051274	chr14:35529529-35724227	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv1048823	chr14:35537281-35724892	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv542032	chr14:35537281-35724892	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv1040540	chr14:35537481-35724753	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv542033	chr14:35537481-35724753	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv1042625	chr14:35546094-35680358	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
17	nsv1050123	chr14:35546114-35724892	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
18	nsv542034	chr14:35546114-35724892	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
19	nsv1050700	chr14:35548276-35639084	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
20	nsv1043692	chr14:35548276-35720016	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
21	nsv1053604	chr14:35548276-35825805	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
22	nsv542035	chr14:35563220-35607117	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
23	nsv1047992	chr14:35563220-35639084	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
24	nsv1052392	chr14:35563220-35893309	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
25	nsv542036	chr14:35563220-35893309	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
26	nsv1053978	chr14:35571762-35639084	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
27	nsv534182	chr14:35579022-35620232	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs941653	PPP2R3C	cis	Whole Blood	GTEx
rs941653	PPP2R3C	Cis_1M	lymphoblastoid	RTeQTL
rs941653	KIAA0391	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35589400-35593000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:35589800-35592600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr14:35589800-35592600	Active TSS	Fetal Brain Female	brain
4	chr14:35589800-35593200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr14:35589800-35595000	Active TSS	K562	blood
6	chr14:35590000-35592600	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr14:35590000-35592800	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr14:35590000-35592800	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr14:35590000-35592800	Active TSS	A549	lung
10	chr14:35590000-35593000	Active TSS	H9 Cell Line	embryonic stem cell
11	chr14:35590000-35593000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:35590200-35592600	Active TSS	H1 Cell Line	embryonic stem cell
13	chr14:35590200-35592600	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr14:35590200-35592600	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr14:35590200-35592600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr14:35590200-35592600	Active TSS	Muscle Satellite Cultured Cells	--
17	chr14:35590200-35592600	Active TSS	Fetal Intestine Small	intestine
18	chr14:35590200-35592600	Active TSS	Left Ventricle	heart
19	chr14:35590200-35592600	Active TSS	Pancreas	Pancrea
20	chr14:35590200-35592600	Active TSS	GM12878-XiMat	blood
21	chr14:35590200-35592600	Active TSS	NHDF-Ad	bronchial
22	chr14:35590200-35592600	Active TSS	NHEK	skin
23	chr14:35590200-35592800	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr14:35590200-35592800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr14:35590200-35592800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr14:35590200-35592800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:35590200-35592800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:35590200-35592800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr14:35590200-35592800	Active TSS	Fetal Intestine Large	intestine
30	chr14:35590200-35592800	Active TSS	Fetal Kidney	kidney
31	chr14:35590200-35592800	Active TSS	Psoas Muscle	Psoas
32	chr14:35590200-35592800	Active TSS	HSMM	muscle
33	chr14:35590200-35593000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr14:35590200-35593000	Active TSS	Right Atrium	heart
35	chr14:35590200-35593000	Active TSS	HSMMtube	muscle
36	chr14:35590200-35593200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:35590200-35593200	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr14:35590200-35593200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr14:35590200-35593400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:35590400-35592600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:35590400-35592600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:35590400-35592600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:35590400-35592600	Active TSS	Fetal Lung	lung
44	chr14:35590400-35592600	Active TSS	Fetal Thymus	thymus
45	chr14:35590400-35592600	Active TSS	Small Intestine	intestine
46	chr14:35590400-35592600	Active TSS	Thymus	Thymus
47	chr14:35590400-35592800	Active TSS	Colonic Mucosa	Colon
48	chr14:35590400-35593000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr14:35590400-35593000	Active TSS	Lung	lung
50	chr14:35590400-35593200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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