Variant report

Variant	rs3132583
Chromosome Location	chr6:30688575-30688576
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	ATF2	chr6:30687634-30688576	GM12878	blood:	n/a	n/a
2	MAX	chr6:30687465-30689845	HCT-116	colon:	n/a	chr6:30689309-30689319 chr6:30689372-30689382 chr6:30689313-30689322
3	MAX	chr6:30688511-30688898	K562	blood:	n/a	n/a
4	POLR2A	chr6:30687422-30690021	H1-neurons	neurons:	n/a	n/a
5	SP1	chr6:30687616-30688782	H1-hESC	embryonic stem cell:	n/a	chr6:30688080-30688092 chr6:30688080-30688092 chr6:30688570-30688584 chr6:30688574-30688583 chr6:30688081-30688090 chr6:30688705-30688719 chr6:30688052-30688066 chr6:30688082-30688091
6	BCLAF1	chr6:30686890-30689854	GM12878	blood:	n/a	chr6:30689371-30689384 chr6:30688101-30688110
7	POLR2A	chr6:30687736-30689679	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr6:30687742-30694690	GM12878	blood:	n/a	n/a
9	CHD1	chr6:30687430-30689809	GM12878	blood:	n/a	n/a
10	SIX5	chr6:30687300-30688798	A549	lung:	n/a	chr6:30687847-30687856 chr6:30687921-30687930 chr6:30687919-30687928
11	MYC	chr6:30688550-30688846	HUVEC	blood vessel:	n/a	n/a
12	POLR2A	chr6:30687413-30689987	HCT-116	colon:	n/a	n/a
13	MAX	chr6:30688514-30689580	H1-hESC	embryonic stem cell:	n/a	chr6:30689309-30689319 chr6:30689372-30689382 chr6:30689313-30689322
14	CREB1	chr6:30688556-30689658	HepG2	liver:	n/a	n/a
15	TBL1XR1	chr6:30687159-30689445	K562	blood:	n/a	n/a
16	CBX3	chr6:30688499-30689617	K562	blood:	n/a	n/a
17	MAX	chr6:30687507-30689656	K562	blood:	n/a	chr6:30689309-30689319 chr6:30689372-30689382 chr6:30689313-30689322
18	POLR2A	chr6:30687036-30695449	HUVEC	blood vessel:	n/a	n/a
19	REST	chr6:30686831-30691010	H1-neurons	neurons:	n/a	chr6:30690432-30690445 chr6:30688079-30688092
20	POLR2A	chr6:30687122-30694167	H1-hESC	embryonic stem cell:	n/a	n/a
21	YY1	chr6:30688514-30688908	K562	blood:	n/a	chr6:30688816-30688830
22	POLR2A	chr6:30683610-30695318	SK-N-MC	brain:	n/a	n/a
23	TAF1	chr6:30687749-30689559	GM12878	blood:	n/a	n/a
24	BCL3	chr6:30687929-30689292	A549	lung:	n/a	chr6:30688101-30688110
25	CHD1	chr6:30687056-30690038	H1-hESC	embryonic stem cell:	n/a	n/a
26	SMC3	chr6:30688496-30688751	K562	blood:	n/a	n/a
27	STAT5A	chr6:30687974-30689487	GM12878	blood:	n/a	chr6:30688745-30688757
28	POLR2A	chr6:30688531-30688929	GM12878	blood:	n/a	n/a
29	MAX	chr6:30687495-30689914	A549	lung:	n/a	chr6:30689309-30689319 chr6:30689372-30689382 chr6:30689313-30689322
30	PML	chr6:30686897-30691157	GM12878	blood:	n/a	chr6:30687409-30687417
31	POLR2A	chr6:30687365-30689684	K562	blood:	n/a	n/a
32	TAF1	chr6:30687558-30689469	ECC-1	luminal epithelium:	n/a	n/a
33	ELF1	chr6:30688543-30688900	K562	blood:	n/a	n/a
34	BHLHE40	chr6:30688539-30688691	GM12878	blood:	n/a	n/a
35	POLR2A	chr6:30687870-30690024	GM12892	blood:	n/a	n/a
36	POLR2A	chr6:30686736-30693839	K562	blood:	n/a	n/a
37	TBP	chr6:30687537-30689600	HepG2	liver:	n/a	n/a
38	POLR2A	chr6:30687488-30695337	Hela-S3	cervix:	n/a	n/a
39	MXI1	chr6:30687176-30689740	GM12878	blood:	n/a	chr6:30689363-30689372
40	POLR2A	chr6:30687144-30689614	Raji	blood:	n/a	n/a
41	PML	chr6:30687574-30689795	K562	blood:	n/a	n/a
42	MYBL2	chr6:30687284-30689915	HepG2	liver:	n/a	n/a
43	NFIC	chr6:30687547-30688848	HepG2	liver:	n/a	n/a
44	NR2F2	chr6:30686803-30689997	K562	blood:	n/a	n/a
45	STAT3	chr6:30688556-30689072	MCF10A-Er-Src	breast:	n/a	chr6:30688745-30688757
46	JUND	chr6:30688491-30688945	A549	lung:	n/a	n/a
47	MBD4	chr6:30687397-30689547	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:30687414-30689375	GM12878	blood:	n/a	n/a
49	ZBTB7A	chr6:30688531-30689664	K562	blood:	n/a	chr6:30689505-30689516
50	JUND	chr6:30687218-30689438	H1-hESC	embryonic stem cell:	n/a	chr6:30689375-30689384 chr6:30688054-30688063 chr6:30689376-30689385

No.	Distal block	Cell Line	Cell type
1	chr6:30687338..30691474-chr6:30850428..30854318,11	MCF-7	breast:
2	chr6:30523499..30526116-chr6:30685040..30688824,4	MCF-7	breast:
3	chr6:30629679..30632498-chr6:30687159..30689670,2	MCF-7	breast:
4	chr6:30455560..30457980-chr6:30688126..30690528,2	K562	blood:
5	chr1:11967939..11969934-chr6:30686668..30688660,2	K562	blood:
6	chr6:30628258..30631199-chr6:30686594..30688662,2	K562	blood:
7	chr6:30613134..30616889-chr6:30684889..30690956,7	MCF-7	breast:
8	chr1:11967863..11968473-chr6:30688369..30689328,2	Hela-S3	cervix:
9	chr22:31365932..31368594-chr6:30687396..30689377,2	K562	blood:
10	chr6:30688404..30690517-chr6:30855397..30858284,2	MCF-7	breast:
11	chr14:36294836..36295834-chr6:30688016..30688899,2	Hela-S3	cervix:
12	chr6:30687707..30689680-chr6:30855398..30858038,2	MCF-7	breast:
13	chr6:30522151..30525852-chr6:30686505..30691954,11	K562	blood:
14	chr6:30576582..30588788-chr6:30682721..30700088,114	K562	blood:
15	chr6:30634661..30668428-chr6:30680318..30698953,145	MCF-7	breast:
16	chr6:30608315..30616989-chr6:30683761..30694958,31	K562	blood:
17	chr6:30591444..30595401-chr6:30685466..30689259,5	K562	blood:
18	chr6:30688042..30689988-chr8:145577489..145580277,2	MCF-7	breast:
19	chr6:30687770..30690244-chr6:30875447..30877174,2	MCF-7	breast:
20	chr15:31283786..31284531-chr6:30688265..30688860,2	Hela-S3	cervix:
21	chr15:60689912..60690621-chr6:30688405..30689136,2	Hela-S3	cervix:
22	chr1:43478758..43479258-chr6:30688143..30689094,2	NB4	blood:
23	chr6:30579743..30580596-chr6:30688361..30688942,2	HCT-116	colon:
24	chr6:30638422..30642374-chr6:30687329..30691225,7	MCF-7	breast:
25	chr11:64884386..64886553-chr6:30687642..30689654,2	MCF-7	breast:
26	chr6:30577862..30587208-chr6:30682997..30696247,43	MCF-7	breast:
27	chr6:30687753..30689397-chr6:36409717..36412070,2	K562	blood:
28	chr1:210547122..210547672-chr6:30687935..30688681,2	Hela-S3	cervix:
29	chr6:30685105..30690458-chr6:30847596..30854595,13	MCF-7	breast:
30	chr6:30590782..30598373-chr6:30685661..30690473,13	MCF-7	breast:
31	chr6:30515029..30517945-chr6:30687848..30689600,2	MCF-7	breast:
32	chr6:30522706..30525361-chr6:30686394..30690570,5	MCF-7	breast:
33	chr6:30455790..30458568-chr6:30687436..30691942,4	MCF-7	breast:
34	chr6:30643326..30660432-chr6:30681522..30696111,127	MCF-7	breast:
35	chr6:30577773..30589670-chr6:30680333..30700280,58	MCF-7	breast:

Variant related genes	Relation type
TUBB	TF binding region
MDC1	TF binding region
ENSG00000230449	Chromatin interaction
ENSG00000271698	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000185803	Chromatin interaction
ENSG00000204580	Chromatin interaction
ENSG00000204560	Chromatin interaction
ENSG00000100916	Chromatin interaction
ENSG00000253352	Chromatin interaction
ENSG00000137343	Chromatin interaction
ENSG00000204564	Chromatin interaction
ENSG00000137411	Chromatin interaction
ENSG00000179165	Chromatin interaction
ENSG00000204590	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000182718	Chromatin interaction
ENSG00000214597	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000204568	Chromatin interaction
ENSG00000174276	Chromatin interaction
ENSG00000204576	Chromatin interaction
ENSG00000266183	Chromatin interaction
ENSG00000222894	Chromatin interaction
ENSG00000112078	Chromatin interaction
ENSG00000213780	Chromatin interaction
ENSG00000137404	Chromatin interaction
ENSG00000166912	Chromatin interaction
ENSG00000146112	Chromatin interaction
ENSG00000255173	Chromatin interaction
ENSG00000204592	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1059612	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1264351	0.83[AMR][1000 genomes]
rs1264373	0.83[AMR][1000 genomes]
rs3094023	0.83[AMR][1000 genomes]
rs3094118	0.85[EUR][1000 genomes]
rs3094125	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3095276	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3095326	0.87[EUR][1000 genomes]
rs3095327	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs3095328	0.89[EUR][1000 genomes]
rs3095332	0.89[EUR][1000 genomes]
rs3095334	0.83[EUR][1000 genomes]
rs3129972	0.90[EUR][1000 genomes]
rs3129973	0.87[EUR][1000 genomes]
rs3129974	0.89[EUR][1000 genomes]
rs3129977	0.82[EUR][1000 genomes]
rs3129978	0.83[EUR][1000 genomes]
rs3129984	0.81[EUR][1000 genomes]
rs3130117	0.83[AMR][1000 genomes]
rs3130247	0.83[AMR][1000 genomes]
rs3130658	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3130660	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3130665	0.85[EUR][1000 genomes]
rs3130668	0.81[EUR][1000 genomes]
rs3130673	0.83[EUR][1000 genomes]
rs3132582	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs3132585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3132599	0.83[EUR][1000 genomes]
rs3132600	0.87[EUR][1000 genomes]
rs3132603	0.83[EUR][1000 genomes]
rs3132605	0.83[EUR][1000 genomes]
rs9262126	0.95[EUR][1000 genomes]
rs9262130	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9262132	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9262135	0.95[EUR][1000 genomes]
rs9262141	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9262142	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9262143	0.92[EUR][1000 genomes]
rs9262146	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' 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	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised 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	967 gene(s)	inside rSNPs	diseases
5	nsv830626	chr6:30558064-30732905	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	406 gene(s)	inside rSNPs	diseases
6	esv2758041	chr6:30644693-30816319	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
7	esv2759413	chr6:30644693-30816319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3132583	HLA-C	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30684400-30690200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr6:30684800-30688800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:30684800-30689600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr6:30685200-30689400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:30686600-30689400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr6:30686600-30689400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:30687000-30689400	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:30687000-30689400	Active TSS	H9 Cell Line	embryonic stem cell
9	chr6:30687000-30689600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:30687000-30689600	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr6:30687000-30690200	Active TSS	GM12878-XiMat	blood
12	chr6:30687000-30690400	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr6:30687200-30688600	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr6:30687200-30689000	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr6:30687200-30689000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr6:30687200-30689200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:30687200-30689400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:30687200-30689400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:30687200-30689400	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr6:30687200-30689400	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr6:30687200-30689400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr6:30687200-30689400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:30687200-30689400	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr6:30687200-30689400	Active TSS	K562	blood
25	chr6:30687200-30689400	Active TSS	NHLF	lung
26	chr6:30687200-30689600	Active TSS	Fetal Intestine Large	intestine
27	chr6:30687200-30689800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:30687200-30690000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr6:30687200-30690000	Active TSS	Aorta	Aorta
30	chr6:30687200-30690200	Active TSS	Lung	lung
31	chr6:30687200-30690200	Active TSS	HSMMtube	muscle
32	chr6:30687200-30690400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:30687200-30690800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:30687400-30689400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:30687400-30689400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:30687400-30689400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:30687400-30689400	Active TSS	Fetal Lung	lung
38	chr6:30687400-30689400	Active TSS	Fetal Stomach	stomach
39	chr6:30687400-30689400	Active TSS	Pancreas	Pancrea
40	chr6:30687400-30689400	Active TSS	A549	lung
41	chr6:30687400-30689600	Active TSS	Stomach Mucosa	stomach
42	chr6:30687400-30689800	Active TSS	Brain Substantia Nigra	brain
43	chr6:30687400-30689800	Active TSS	Spleen	Spleen
44	chr6:30687400-30689800	Active TSS	NHDF-Ad	bronchial
45	chr6:30687400-30690000	Active TSS	Ovary	ovary
46	chr6:30687400-30690000	Active TSS	Sigmoid Colon	Sigmoid Colon
47	chr6:30687400-30690200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:30687400-30690200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:30687400-30690200	Active TSS	Esophagus	oesophagus
50	chr6:30687400-30690400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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