Variant report

Variant	rs11767726
Chromosome Location	chr7:150018096-150018097
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr7:150017946-150018500	K562	blood:	n/a	n/a
2	HDAC2	chr7:150018027-150018484	HepG2	liver:	n/a	n/a
3	RCOR1	chr7:150017994-150018440	K562	blood:	n/a	n/a
4	CEBPB	chr7:150018066-150018552	K562	blood:	n/a	chr7:150018348-150018359
5	BATF	chr7:150017858-150018347	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:150018091-150018531	Hela-S3	cervix:	n/a	chr7:150018348-150018359
7	IRF1	chr7:150017891-150018359	K562	blood:	n/a	n/a
8	FOS	chr7:150018077-150018520	MCF10A-Er-Src	breast:	n/a	n/a
9	MAX	chr7:150017917-150018285	K562	blood:	n/a	n/a
10	GATA3	chr7:150017844-150018358	T-47D	breast:	n/a	n/a
11	STAT5A	chr7:150017859-150018299	GM12878	blood:	n/a	n/a
12	MYC	chr7:150017984-150018417	K562	blood:	n/a	n/a
13	POLR2A	chr7:150017791-150018337	GM12892	blood:	n/a	n/a
14	STAT3	chr7:150018048-150018395	MCF10A-Er-Src	breast:	n/a	n/a
15	TEAD4	chr7:150017730-150018527	K562	blood:	n/a	n/a
16	MAFK	chr7:150017958-150018438	Hela-S3	cervix:	n/a	chr7:150018156-150018171
17	UBTF	chr7:150018067-150018367	K562	blood:	n/a	n/a
18	EP300	chr7:150018020-150018456	K562	blood:	n/a	n/a
19	MTA3	chr7:150017854-150018449	GM12878	blood:	n/a	n/a
20	ARID3A	chr7:150017975-150018386	K562	blood:	n/a	n/a
21	NRF1	chr7:150017845-150018407	K562	blood:	n/a	n/a
22	NR2F2	chr7:150017863-150018477	K562	blood:	n/a	n/a
23	PML	chr7:150017893-150018490	K562	blood:	n/a	n/a
24	CEBPB	chr7:150018042-150018573	MCF-7	breast:	n/a	chr7:150018348-150018359
25	CEBPB	chr7:150018075-150018553	K562	blood:	n/a	chr7:150018348-150018359
26	CBX3	chr7:150017759-150018584	K562	blood:	n/a	n/a
27	POLR2A	chr7:150017554-150018744	HepG2	liver:	n/a	n/a
28	TBP	chr7:150018008-150018312	K562	blood:	n/a	n/a
29	EP300	chr7:150018019-150018527	HepG2	liver:	n/a	n/a
30	MAFK	chr7:150017978-150018376	HepG2	liver:	n/a	chr7:150018156-150018171
31	MAFK	chr7:150017704-150018651	GM12878	blood:	n/a	chr7:150018156-150018171
32	EP300	chr7:150018006-150018412	GM12878	blood:	n/a	n/a
33	EP300	chr7:150017899-150018433	K562	blood:	n/a	n/a
34	EP300	chr7:150018086-150018430	Hela-S3	cervix:	n/a	n/a
35	MYC	chr7:150017950-150018444	MCF10A-Er-Src	breast:	n/a	n/a
36	BACH1	chr7:150018015-150018253	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr7:150018009-150018378	K562	blood:	n/a	n/a
38	BCLAF1	chr7:150017851-150018345	GM12878	blood:	n/a	n/a
39	FOS	chr7:150018082-150018365	MCF10A-Er-Src	breast:	n/a	n/a
40	JUN	chr7:150017978-150018574	K562	blood:	n/a	n/a
41	MAFK	chr7:150017887-150018457	K562	blood:	n/a	chr7:150018156-150018171
42	CEBPB	chr7:150017903-150018553	K562	blood:	n/a	chr7:150018348-150018359
43	POLR2A	chr7:150017951-150018435	K562	blood:	n/a	n/a
44	USF2	chr7:150018063-150018304	Hela-S3	cervix:	n/a	n/a
45	MAFK	chr7:150017988-150018375	HepG2	liver:	n/a	chr7:150018156-150018171
46	POLR2A	chr7:150017841-150018253	GM12891	blood:	n/a	n/a
47	NFATC1	chr7:150017844-150018500	GM12878	blood:	n/a	n/a
48	ATF2	chr7:150017882-150018408	GM12878	blood:	n/a	n/a
49	STAT3	chr7:150018039-150018395	MCF10A-Er-Src	breast:	n/a	n/a
50	TBL1XR1	chr7:150018094-150018354	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150018095-150018145	Caco-2	colon:	n/a
2	chr7:150018095-150018145	PANC-1	pancreas:	n/a
3	chr7:150018095-150018145	HCPEpiC	choroid plexus:	n/a
4	chr7:150018095-150018145	MCF-7	breast:	n/a
5	chr7:150018095-150018145	GM06990	blood:	n/a
6	chr7:150018095-150018145	PFSK-1	brain:	n/a
7	chr7:150018095-150018145	NHDF-neo	bronchial:	n/a
8	chr7:150018095-150018145	AoSMC	blood vessel:	n/a
9	chr7:150018095-150018145	BJ	skin:	n/a
10	chr7:150018095-150018145	HAEpiC	amniotic membrane:	n/a
11	chr7:150018095-150018145	GM12892	blood:	n/a
12	chr7:150018095-150018145	Hepatocyte	liver:	n/a
13	chr7:150018095-150018145	HMEC	breast:	n/a
14	chr7:150018095-150018145	AG09309	skin:	n/a
15	chr7:150018095-150018145	SK-N-SH	brain:	n/a
16	chr7:150018095-150018145	CMK	blood:	n/a
17	chr7:150018095-150018145	PrEC	prostate:	n/a
18	chr7:150018095-150018145	HRCEpiC	kidney:	n/a
19	chr7:150018095-150018145	BE2_C	brain:	n/a
20	chr7:150018095-150018145	NT2-D1	testis:	n/a
21	chr7:150018095-150018145	HIPEpiC	eye:	n/a
22	chr7:150018095-150018145	NHBE	bronchial:	n/a
23	chr7:150018095-150018145	HNPCEpiC	eye:	n/a
24	chr7:150018095-150018145	AG09319	gingival:	n/a
25	chr7:150018095-150018145	NB4	blood:	n/a
26	chr7:150018095-150018145	U87	brain:	n/a
27	chr7:150018095-150018145	HCT-116	colon:	n/a
28	chr7:150018095-150018145	GM12878	blood:	n/a
29	chr7:150018095-150018145	T-47D	breast:	n/a
30	chr7:150018095-150018145	ECC-1	luminal epithelium:	n/a
31	chr7:150018095-150018145	HUVEC	blood vessel:	n/a
32	chr7:150018095-150018145	Hela-S3	cervix:	n/a
33	chr7:150018095-150018145	LNCaP	prostate:	n/a
34	chr7:150018095-150018145	HCF	heart:	n/a
35	chr7:150018095-150018145	GM12891	blood:	n/a
36	chr7:150018095-150018145	MCF10A-Er-Src	breast:	n/a
37	chr7:150018095-150018145	SK-N-MC	brain:	n/a
38	chr7:150018095-150018145	HCM	heart:	n/a
39	chr7:150018095-150018145	IMR90	lung:	fetal
40	chr7:150018095-150018145	AG10803	skin:	n/a
41	chr7:150018095-150018145	SAEC	small airway:	n/a
42	chr7:150018095-150018145	HRPEpiC	eye:	n/a
43	chr7:150018095-150018145	AG04450	lung:	fetal
44	chr7:150018095-150018145	HL-60	blood:	n/a
45	chr7:150018095-150018145	NH-A	brain:	n/a
46	chr7:150018095-150018145	HRE	kidney:	n/a
47	chr7:150018095-150018145	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:150018095-150018145	HepG2	liver:	n/a
49	chr7:150018095-150018145	A549	lung:	n/a
50	chr7:150018095-150018145	AG04449	skin:	fetal

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150017186..150022010-chr7:150063447..150067622,10	K562	blood:
2	chr7:150016171..150021897-chr7:150062899..150068795,19	MCF-7	breast:
3	chr7:150017073..150026383-chr7:150074145..150079980,13	MCF-7	breast:
4	chr7:150011196..150014151-chr7:150016910..150019220,3	MCF-7	breast:
5	chr7:150017660..150019696-chr7:150021703..150024720,3	MCF-7	breast:
6	chr7:150015754..150018552-chr7:150022043..150024814,2	MCF-7	breast:
7	chr7:150015545..150018371-chr7:150018521..150022002,4	MCF-7	breast:
8	chr7:150017819..150020177-chr7:150077421..150080084,2	MCF-7	breast:
9	chr7:150017344..150021301-chr7:150099535..150103707,10	K562	blood:
10	chr7:150016043..150018728-chr7:150071723..150073696,2	MCF-7	breast:
11	chr7:150011128..150013458-chr7:150017252..150018942,2	MCF-7	breast:
12	chr7:150016446..150018907-chr7:150027927..150030542,2	MCF-7	breast:
13	chr7:150017186..150022141-chr7:150063447..150068849,12	K562	blood:
14	chr7:150016641..150019534-chr7:150075821..150077666,2	K562	blood:
15	chr7:150016445..150018121-chr7:150116375..150118836,2	K562	blood:
16	chr7:150015287..150018843-chr7:150110338..150114504,3	K562	blood:

No data

Variant related genes	Relation type
LRRC61	TF binding region
LRRC61	CpG island
ENSG00000127399	Chromatin interaction
ENSG00000106526	Chromatin interaction
ENSG00000214022	Chromatin interaction
ENSG00000196456	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 28 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1047207	0.81[EUR][1000 genomes]
rs1047575	0.84[CEU][hapmap]
rs10952249	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10952250	0.90[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1132261	0.91[JPT][hapmap]
rs11764936	0.90[CEU][hapmap];0.88[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11765644	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11765692	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11766288	0.86[EUR][1000 genomes]
rs11769348	0.90[CEU][hapmap];0.88[MEX][hapmap];0.89[TSI][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11773351	0.87[EUR][1000 genomes]
rs11974980	0.95[CEU][hapmap];0.85[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11975886	0.94[CEU][hapmap];0.83[CHB][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11983355	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1464752	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1464753	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17173617	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs17173681	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs17173682	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs17837498	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1916932	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1962004	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1983440	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2108851	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108852	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108853	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108854	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2159234	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2159235	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2159236	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2373751	0.88[EUR][1000 genomes]
rs3088207	0.86[EUR][1000 genomes]
rs3735167	0.84[CEU][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes]
rs3735169	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs3735170	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs3735171	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs3735172	0.90[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3735173	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3735174	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3735175	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3800780	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3800781	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4395803	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4554381	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55715989	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55881542	0.88[EUR][1000 genomes]
rs55974958	0.81[EUR][1000 genomes]
rs56019796	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56190213	0.88[EUR][1000 genomes]
rs56923535	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56998970	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57888387	0.88[EUR][1000 genomes]
rs59572505	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60268791	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60283368	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60467296	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61421252	0.81[EUR][1000 genomes]
rs73170169	0.88[EUR][1000 genomes]
rs73170174	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73170185	0.88[EUR][1000 genomes]
rs7781827	0.95[CEU][hapmap];0.80[CHB][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7788316	0.95[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7800196	0.84[CEU][hapmap]
rs7806429	0.95[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription 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	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv508490	chr7:150006068-150051241	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv889453	chr7:150009838-150104410	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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 target site	50 gene(s)	inside rSNPs	diseases
6	nsv889454	chr7:150009838-150115183	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv889455	chr7:150013393-150104410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS 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 target site	50 gene(s)	inside rSNPs	diseases
8	nsv889456	chr7:150013393-150115183	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases

mRNA abundance (count:28)

SNP	Gene	Cis/trans	Tissue	Source
rs11767726	RARRES2	cis	normal skin	skin_eQTL
rs11767726	REPIN1	cis	Muscle Skeletal	GTEx
rs11767726	LRRC61	cis	lung	GTEx
rs11767726	ZBED6CL	cis	Esophagus Muscularis	GTEx
rs11767726	LRRC61	cis	Whole Blood	GTEx
rs11767726	ACTR3C	cis	Muscle Skeletal	GTEx
rs11767726		cis	Lymphoblastoid	GTEx
rs11767726	LRRC61	cis	multi-tissue	Pritchard
rs11767726	LRRC61	cis	parietal	SCAN
rs11767726	LRRC61	cis	Nerve Tibial	GTEx
rs11767726	C7orf29	cis	lymphoblastoid	seeQTL
rs11767726	RARRES2	cis	multi-tissue	Pritchard
rs11767726	LRRC61	cis	lymphoblastoid	seeQTL
rs11767726	LRRC61	cis	cerebellum	SCAN
rs11767726	LRRC61	cis	Artery Tibial	GTEx
rs11767726	LRRC61	cis	Esophagus Mucosa	GTEx
rs11767726	LRRC61	cis	Skin Sun Exposed Lower leg	GTEx
rs11767726	LRRC61	cis	Adipose Subcutaneous	GTEx
rs11767726	RARRES2	cis	lymphoblastoid	seeQTL
rs11767726	LRRC61	cis	Heart Left Ventricle	GTEx
rs11767726	RARRES2	cis	brain	seeQTL
rs11767726	LRRC61	cis	Thyroid	GTEx
rs11767726	MGC3036	cis	multi-tissue	Pritchard
rs11767726	SAMD14	cis	Liver	GTEx
rs11767726	LRRC61	cis	Artery Aorta	GTEx
rs11767726	LRRC61	cis	Muscle Skeletal	GTEx
rs11767726	ZBED6CL	cis	Esophagus Mucosa	GTEx
rs11767726	RARRES2	trans	brain	seeQTL

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149984200-150019400	Weak transcription	Colonic Mucosa	Colon
2	chr7:150004000-150019000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:150009400-150020000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:150010400-150018200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:150011000-150019000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:150011000-150019600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:150011200-150019200	Weak transcription	Spleen	Spleen
8	chr7:150011400-150019000	Weak transcription	Gastric	stomach
9	chr7:150011600-150019000	Weak transcription	Stomach Mucosa	stomach
10	chr7:150012800-150019000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:150013200-150019200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:150014000-150019000	Weak transcription	Primary T cells from cord blood	blood
13	chr7:150014000-150019200	Weak transcription	Primary B cells from cord blood	blood
14	chr7:150014200-150018200	Weak transcription	NHLF	lung
15	chr7:150014400-150018200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr7:150015000-150019000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr7:150015000-150019200	Weak transcription	Thymus	Thymus
18	chr7:150015000-150019400	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr7:150015200-150018200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr7:150015200-150019000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:150015200-150019000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr7:150015200-150019600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:150015400-150019000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr7:150015400-150020200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:150015600-150019200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:150015600-150019400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr7:150015600-150019400	Weak transcription	NHEK	skin
28	chr7:150016000-150019000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:150016200-150019800	Enhancers	Placenta	Placenta
30	chr7:150016400-150019000	Enhancers	Liver	Liver
31	chr7:150016400-150019000	Enhancers	Pancreas	Pancrea
32	chr7:150016600-150019000	Weak transcription	Primary B cells from peripheral blood	blood
33	chr7:150016600-150019200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr7:150016800-150018800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:150016800-150019200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:150017000-150019000	Weak transcription	Esophagus	oesophagus
37	chr7:150017000-150019200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:150017000-150019600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:150017000-150019600	Weak transcription	Fetal Muscle Leg	muscle
40	chr7:150017200-150018800	Weak transcription	Dnd41	blood
41	chr7:150017400-150020000	Weak transcription	HUVEC	blood vessel
42	chr7:150017600-150019200	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr7:150017800-150018200	Enhancers	HSMM	muscle
44	chr7:150017800-150018200	Transcr. at gene 5' and 3'	K562	blood
45	chr7:150017800-150018600	Flanking Active TSS	GM12878-XiMat	blood
46	chr7:150017800-150019000	Enhancers	HepG2	liver
47	chr7:150017800-150019400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:150017800-150019800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:150018000-150018200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:150018000-150018200	Enhancers	Psoas Muscle	Psoas

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