Variant report

Variant	rs56186064
Chromosome Location	chr11:64510756-64510757
allele	C/T
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	SPI1	chr11:64510405-64511350	HL-60	blood:	n/a	n/a
2	RAD21	chr11:64510133-64512065	SK-N-SH	brain:	n/a	chr11:64511012-64511025 chr11:64510945-64510958 chr11:64511205-64511217 chr11:64511203-64511222 chr11:64512029-64512041
3	TEAD4	chr11:64510611-64511743	ECC-1	luminal epithelium:	n/a	n/a
4	MAZ	chr11:64509811-64513853	K562	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64510447-64510457 chr11:64513619-64513629 chr11:64513719-64513729
5	CTCF	chr11:64510350-64510775	GM19239	blood:	n/a	chr11:64510690-64510703 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510497-64510506
6	MAX	chr11:64510024-64510976	ECC-1	luminal epithelium:	n/a	chr11:64510447-64510457
7	CTCF	chr11:64510749-64510821	GM10248	blood:	n/a	n/a
8	CTCF	chr11:64510680-64510830	A549	lung:	n/a	chr11:64510690-64510703
9	YY1	chr11:64510220-64510762	HepG2	liver:	n/a	chr11:64510524-64510533
10	CTBP2	chr11:64509270-64511435	H1-hESC	embryonic stem cell:	n/a	n/a
11	TEAD4	chr11:64510744-64511262	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr11:64510370-64510768	Raji	blood:	n/a	n/a
13	FOXM1	chr11:64510207-64510810	GM12878	blood:	n/a	n/a
14	CTCF	chr11:64510247-64510801	MCF-7	breast:	n/a	chr11:64510690-64510703 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510497-64510506
15	HCFC1	chr11:64509885-64511318	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:64510330-64510798	ECC-1	luminal epithelium:	n/a	chr11:64510562-64510573
17	MAX	chr11:64509884-64513844	K562	blood:	n/a	chr11:64512748-64512757 chr11:64512445-64512454 chr11:64512631-64512641 chr11:64510447-64510457 chr11:64513619-64513629 chr11:64513719-64513729
18	MYC	chr11:64510352-64511985	K562	blood:	n/a	chr11:64510447-64510457
19	TEAD4	chr11:64510709-64511352	K562	blood:	n/a	n/a
20	TEAD4	chr11:64510756-64511224	H1-hESC	embryonic stem cell:	n/a	n/a
21	RCOR1	chr11:64510394-64511568	GM12878	blood:	n/a	n/a
22	CEBPB	chr11:64510381-64510756	A549	lung:	n/a	chr11:64510562-64510573
23	CEBPB	chr11:64510254-64510931	A549	lung:	n/a	chr11:64510562-64510573
24	CTCF	chr11:64510711-64510872	GM19240	blood:	n/a	n/a
25	MAZ	chr11:64509820-64511530	IMR90	lung:	n/a	chr11:64510447-64510457
26	CHD2	chr11:64510352-64510959	Hela-S3	cervix:	n/a	chr11:64510479-64510489 chr11:64510711-64510721 chr11:64510899-64510909
27	SMC3	chr11:64510149-64511691	SK-N-SH	brain:	n/a	chr11:64510493-64510507
28	POLR2A	chr11:64508984-64513948	HL-60	blood:	n/a	n/a
29	CTCF	chr11:64510221-64511558	HCT-116	colon:	n/a	chr11:64511203-64511219 chr11:64510949-64510958 chr11:64510690-64510703 chr11:64511202-64511220 chr11:64511205-64511218 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510946-64510959 chr11:64511205-64511218 chr11:64510497-64510506
30	CEBPB	chr11:64510375-64510756	HepG2	liver:	n/a	chr11:64510562-64510573
31	NR2F2	chr11:64510379-64510964	K562	blood:	n/a	n/a
32	JUND	chr11:64510374-64511531	K562	blood:	n/a	chr11:64510482-64510491
33	RCOR1	chr11:64509845-64512147	K562	blood:	n/a	n/a
34	TFAP2A	chr11:64510190-64511319	Hela-S3	cervix:	n/a	chr11:64510826-64510840 chr11:64510826-64510840 chr11:64510962-64510973 chr11:64510962-64510973 chr11:64510947-64510959 chr11:64510461-64510473 chr11:64510826-64510840 chr11:64510962-64510973 chr11:64510828-64510838 chr11:64510461-64510473 chr11:64510461-64510473 chr11:64510828-64510838 chr11:64510962-64510973 chr11:64510947-64510959 chr11:64510828-64510838 chr11:64510461-64510473 chr11:64510463-64510478
35	CEBPB	chr11:64510403-64510797	ECC-1	luminal epithelium:	n/a	chr11:64510562-64510573
36	ZBTB7A	chr11:64510181-64511804	K562	blood:	n/a	chr11:64510902-64510911
37	MAX	chr11:64509967-64512087	A549	lung:	n/a	chr11:64510447-64510457
38	ZMIZ1	chr11:64510264-64511499	K562	blood:	n/a	n/a
39	POLR2A	chr11:64510731-64510787	H1-hESC	embryonic stem cell:	n/a	n/a
40	TCF12	chr11:64510330-64511333	ECC-1	luminal epithelium:	n/a	n/a
41	MAX	chr11:64509818-64510832	NB4	blood:	n/a	chr11:64510447-64510457
42	CEBPB	chr11:64510455-64510760	A549	lung:	n/a	chr11:64510562-64510573
43	RAD21	chr11:64509913-64511625	HCT-116	colon:	n/a	chr11:64511012-64511025 chr11:64510945-64510958 chr11:64511205-64511217 chr11:64511203-64511222
44	RAD21	chr11:64510197-64510811	H1-hESC	embryonic stem cell:	n/a	n/a
45	ESRRA	chr11:64509625-64512230	GM12878	blood:	n/a	chr11:64511737-64511750
46	POLR2A	chr11:64510220-64513732	NB4	blood:	n/a	n/a
47	EGR1	chr11:64510294-64511277	K562	blood:	n/a	chr11:64510902-64510915 chr11:64510716-64510729 chr11:64511076-64511087 chr11:64511186-64511195
48	CTCF	chr11:64509969-64512104	SK-N-SH	brain:	n/a	chr11:64511203-64511219 chr11:64510949-64510958 chr11:64510690-64510703 chr11:64511985-64511998 chr11:64511202-64511220 chr11:64511205-64511218 chr11:64510494-64510504 chr11:64510492-64510508 chr11:64510491-64510509 chr11:64510946-64510959 chr11:64511205-64511218 chr11:64510497-64510506
49	NR2F2	chr11:64509733-64511710	K562	blood:	n/a	n/a
50	ZBTB7A	chr11:64510226-64512265	ECC-1	luminal epithelium:	n/a	chr11:64510902-64510911

No.	Distal block	Cell Line	Cell type
1	chr11:64508515..64511238-chr11:64521497..64525046,4	MCF-7	breast:
2	chr11:64420673..64421273-chr11:64510420..64510982,3	MCF-7	breast:
3	chr11:64509047..64511433-chr11:64527648..64529214,2	MCF-7	breast:
4	chr11:64507790..64516181-chr11:64524582..64537783,30	K562	blood:
5	chr11:64510149..64512039-chr11:64538219..64540894,2	MCF-7	breast:
6	chr11:64510615..64511340-chr17:46047851..46048383,2	MCF-7	breast:
7	chr11:64503034..64505808-chr11:64508705..64511765,4	MCF-7	breast:
8	chr11:64506030..64508610-chr11:64510560..64513523,3	MCF-7	breast:
9	chr11:64489351..64492621-chr11:64507509..64512935,5	K562	blood:
10	chr11:64124497..64126994-chr11:64509396..64512374,2	K562	blood:
11	chr11:64509857..64513722-chr11:64571129..64574033,3	MCF-7	breast:
12	chr11:64509755..64511903-chr11:65684738..65686627,2	K562	blood:
13	chr11:64510354..64515027-chr11:64543156..64548358,11	K562	blood:
14	chr11:64489616..64492284-chr11:64509871..64511516,3	K562	blood:
15	chr11:64509463..64511820-chr11:64545145..64547148,2	MCF-7	breast:
16	chr11:64490496..64491176-chr11:64510209..64510932,2	MCF-7	breast:

Variant related genes	Relation type
RASGRP2	TF binding region
ENSG00000110076	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000133895	Chromatin interaction
ENSG00000068831	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000068976	Chromatin interaction
ENSG00000108465	Chromatin interaction
ENSG00000168066	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10466694	1.00[EUR][1000 genomes]
rs11231806	1.00[EUR][1000 genomes]
rs11231811	1.00[EUR][1000 genomes]
rs11231812	1.00[EUR][1000 genomes]
rs11231865	1.00[EUR][1000 genomes]
rs11231866	1.00[EUR][1000 genomes]
rs11821081	1.00[EUR][1000 genomes]
rs1212539	1.00[EUR][1000 genomes]
rs1212851	1.00[EUR][1000 genomes]
rs12273948	1.00[EUR][1000 genomes]
rs12281931	1.00[EUR][1000 genomes]
rs12293573	1.00[EUR][1000 genomes]
rs17146100	1.00[EUR][1000 genomes]
rs17146110	1.00[EUR][1000 genomes]
rs1787671	1.00[EUR][1000 genomes]
rs2022049	1.00[EUR][1000 genomes]
rs2518908	1.00[EUR][1000 genomes]
rs2666561	1.00[EUR][1000 genomes]
rs2666562	1.00[EUR][1000 genomes]
rs2904961	1.00[EUR][1000 genomes]
rs2959651	1.00[EUR][1000 genomes]
rs3016758	1.00[EUR][1000 genomes]
rs41323046	1.00[EUR][1000 genomes]
rs475704	1.00[EUR][1000 genomes]
rs512926	1.00[EUR][1000 genomes]
rs516041	1.00[EUR][1000 genomes]
rs534073	1.00[EUR][1000 genomes]
rs535606	1.00[EUR][1000 genomes]
rs541305	1.00[EUR][1000 genomes]
rs545167	1.00[EUR][1000 genomes]
rs545819	1.00[EUR][1000 genomes]
rs546323	1.00[EUR][1000 genomes]
rs550930	1.00[EUR][1000 genomes]
rs553618	1.00[EUR][1000 genomes]
rs559095	1.00[EUR][1000 genomes]
rs559977	1.00[EUR][1000 genomes]
rs565688	1.00[EUR][1000 genomes]
rs573545	1.00[EUR][1000 genomes]
rs579175	1.00[EUR][1000 genomes]
rs58571986	1.00[EUR][1000 genomes]
rs6591863	1.00[EUR][1000 genomes]
rs7110778	1.00[EUR][1000 genomes]
rs7113097	1.00[EUR][1000 genomes]
rs7127435	1.00[EUR][1000 genomes]
rs73492139	1.00[EUR][1000 genomes]
rs73492140	1.00[EUR][1000 genomes]
rs73492144	1.00[EUR][1000 genomes]
rs73494206	1.00[EUR][1000 genomes]
rs7948607	1.00[EUR][1000 genomes]
rs7948832	1.00[EUR][1000 genomes]
rs9326433	1.00[EUR][1000 genomes]
rs9326434	1.00[EUR][1000 genomes]
rs9666331	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking 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 target site	75 gene(s)	inside rSNPs	diseases
5	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
6	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
8	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv897697	chr11:64447420-64584959	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
12	nsv897698	chr11:64447420-64621573	Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS 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 target site	82 gene(s)	inside rSNPs	diseases
13	nsv897699	chr11:64447420-64638041	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
14	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription 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	1071 gene(s)	inside rSNPs	diseases
15	nsv555202	chr11:64477050-64573589	Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
16	nsv468597	chr11:64477050-64584959	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
17	nsv468598	chr11:64477050-64584959	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
18	nsv555203	chr11:64477050-64584959	Strong transcription Genic enhancers Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
19	nsv1049744	chr11:64486615-64630149	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
20	nsv832189	chr11:64487183-64620199	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
21	nsv897701	chr11:64501991-64520569	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64508600-64513000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr11:64508800-64512000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr11:64509000-64511400	Active TSS	H9 Cell Line	embryonic stem cell
4	chr11:64509000-64512000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
5	chr11:64509200-64511200	Flanking Active TSS	Stomach Smooth Muscle	stomach
6	chr11:64509200-64511800	Bivalent Enhancer	Fetal Brain Male	brain
7	chr11:64509200-64512000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:64509200-64512000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr11:64509200-64512600	Active TSS	Brain Anterior Caudate	brain
10	chr11:64509400-64511000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:64509400-64511200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:64509400-64511200	Active TSS	Brain Substantia Nigra	brain
13	chr11:64509400-64511200	Active TSS	Rectal Smooth Muscle	rectum
14	chr11:64509400-64511800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:64509400-64512000	Flanking Active TSS	Primary B cells from cord blood	blood
16	chr11:64509400-64512000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
17	chr11:64509400-64512000	Flanking Active TSS	Right Ventricle	heart
18	chr11:64509400-64512000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr11:64509400-64512200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:64509400-64513600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr11:64509600-64510800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr11:64509600-64510800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:64509600-64510800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
24	chr11:64509600-64510800	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr11:64509600-64511000	Flanking Active TSS	Placenta	Placenta
26	chr11:64509600-64511200	Enhancers	Dnd41	blood
27	chr11:64509600-64511400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
28	chr11:64509600-64511400	Active TSS	Psoas Muscle	Psoas
29	chr11:64509600-64511600	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:64509600-64511600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:64509600-64511800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:64509600-64512000	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr11:64509600-64512000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:64509600-64512000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
35	chr11:64509600-64512000	Flanking Active TSS	Spleen	Spleen
36	chr11:64509600-64512200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
37	chr11:64509600-64512400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:64509600-64512600	Enhancers	Fetal Heart	heart
39	chr11:64509600-64513600	Active TSS	Left Ventricle	heart
40	chr11:64509800-64510800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:64509800-64510800	Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr11:64509800-64511000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr11:64509800-64511400	Active TSS	Small Intestine	intestine
44	chr11:64509800-64512000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr11:64509800-64513200	Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr11:64509800-64513600	Active TSS	Right Atrium	heart
47	chr11:64509800-64514000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr11:64510000-64510800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:64510000-64510800	Bivalent/Poised TSS	HSMM	muscle
50	chr11:64510000-64511000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links