Variant report

Variant	rs535957724
Chromosome Location	chr11:67141827-67141828
allele	A/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	POLR2A	chr11:67141207-67142366	A549	lung:	n/a	n/a
2	CTCF	chr11:67141720-67141870	GM12867	blood:	n/a	n/a
3	RAD21	chr11:67141520-67142056	A549	lung:	n/a	chr11:67141687-67141697 chr11:67141800-67141812
4	POLR2A	chr11:67140056-67142142	SK-N-SH	brain:	n/a	n/a
5	CTCF	chr11:67141720-67141870	GM12874	blood:	n/a	n/a
6	EP300	chr11:67140889-67143973	A549	lung:	n/a	chr11:67141604-67141611 chr11:67143538-67143554 chr11:67140948-67140964 chr11:67141185-67141199
7	CTCF	chr11:67141820-67141970	HCM	heart:	n/a	n/a
8	CTCF	chr11:67141536-67142133	SK-N-SH	brain:	n/a	n/a
9	ZC3H11A	chr11:67141461-67141911	K562	blood:	n/a	n/a
10	SIX5	chr11:67140867-67142749	A549	lung:	n/a	chr11:67141928-67141937
11	MAX	chr11:67141380-67142614	A549	lung:	n/a	n/a
12	CTCF	chr11:67141760-67141910	NHDF-neo	bronchial:	n/a	n/a
13	EP300	chr11:67141059-67142259	ECC-1	luminal epithelium:	n/a	chr11:67141604-67141611 chr11:67141185-67141199
14	MAX	chr11:67141410-67142269	MCF-7	breast:	n/a	n/a
15	HDAC2	chr11:67141526-67142069	MCF-7	breast:	n/a	n/a
16	SIN3AK20	chr11:67139835-67142256	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:67141700-67141850	GM12872	blood:	n/a	n/a
18	STAT3	chr11:67141789-67141989	MCF10A-Er-Src	breast:	n/a	chr11:67141819-67141831 chr11:67141793-67141805
19	EP300	chr11:67141636-67142150	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:67140037-67142665	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr11:67141700-67141850	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr11:67141717-67141892	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr11:67141330-67142359	A549	lung:	n/a	chr11:67141369-67141378
24	RAD21	chr11:67141597-67141904	K562	blood:	n/a	chr11:67141687-67141697 chr11:67141800-67141812
25	CTCF	chr11:67141720-67141870	K562	blood:	n/a	n/a
26	CTCF	chr11:67141680-67141830	GM06990	blood:	n/a	n/a
27	NR3C1	chr11:67141498-67142203	A549	lung:	n/a	chr11:67141991-67142000 chr11:67141992-67142001
28	PBX3	chr11:67140994-67142227	SK-N-SH	brain:	n/a	n/a
29	CTCF	chr11:67141720-67141870	GM12871	blood:	n/a	n/a
30	CREB1	chr11:67140861-67142257	A549	lung:	n/a	n/a
31	FOXA2	chr11:67141025-67142703	A549	lung:	n/a	chr11:67142411-67142423
32	HMGN3	chr11:67141352-67141920	K562	blood:	n/a	n/a
33	MYC	chr11:67141746-67141982	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr11:67141679-67141909	GM19240	blood:	n/a	n/a
35	CTCF	chr11:67141740-67141890	GM06990	blood:	n/a	n/a
36	EP300	chr11:67140327-67143351	ECC-1	luminal epithelium:	n/a	chr11:67141604-67141611 chr11:67140948-67140964 chr11:67141185-67141199 chr11:67140686-67140702
37	SP1	chr11:67140841-67144091	A549	lung:	n/a	chr11:67143748-67143762 chr11:67141289-67141303 chr11:67141574-67141588 chr11:67141470-67141484 chr11:67141363-67141372 chr11:67141370-67141379 chr11:67141258-67141272 chr11:67141368-67141380 chr11:67140960-67140974 chr11:67140956-67140968 chr11:67143704-67143718 chr11:67141262-67141276 chr11:67143744-67143753 chr11:67141362-67141374 chr11:67142152-67142166 chr11:67141462-67141474 chr11:67142824-67142838 chr11:67140957-67140966 chr11:67142668-67142677 chr11:67143749-67143758 chr11:67141369-67141378 chr11:67141462-67141474 chr11:67140958-67140967 chr11:67141362-67141374 chr11:67141463-67141472 chr11:67141255-67141269 chr11:67142658-67142670 chr11:67142659-67142668 chr11:67142655-67142669 chr11:67142659-67142669 chr11:67141365-67141379 chr11:67141370-67141379 chr11:67143743-67143757 chr11:67141244-67141258 chr11:67141368-67141380 chr11:67142658-67142670 chr11:67140956-67140968
38	STAT3	chr11:67141579-67142137	MCF10A-Er-Src	breast:	n/a	chr11:67141819-67141831 chr11:67141793-67141805
39	STAT3	chr11:67141599-67142027	MCF10A-Er-Src	breast:	n/a	chr11:67141819-67141831 chr11:67141793-67141805
40	TEAD4	chr11:67141524-67142259	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr11:67140890-67142772	A549	lung:	n/a	n/a
42	MYC	chr11:67141667-67142028	K562	blood:	n/a	n/a
43	MYC	chr11:67141589-67142216	K562	blood:	n/a	n/a
44	TEAD4	chr11:67141494-67142203	K562	blood:	n/a	n/a
45	ELF1	chr11:67141647-67142087	A549	lung:	n/a	n/a
46	JUND	chr11:67141614-67142137	HepG2	liver:	n/a	chr11:67141685-67141694 chr11:67141991-67142001 chr11:67141990-67142002 chr11:67141990-67142001 chr11:67141992-67142000 chr11:67141993-67142004 chr11:67141991-67142001 chr11:67141991-67142001
47	CTCF	chr11:67141740-67141890	AG09319	gingival:	n/a	n/a
48	CTCF	chr11:67141720-67141870	HRE	kidney:	n/a	n/a
49	MAX	chr11:67141159-67142664	ECC-1	luminal epithelium:	n/a	chr11:67141256-67141266 chr11:67141367-67141377
50	CTCF	chr11:67141760-67141910	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67141792-67141842	HCF	heart:	n/a
2	chr11:67141792-67141842	SK-N-SH_RA	brain:	n/a
3	chr11:67141792-67141842	ECC-1	luminal epithelium:	n/a
4	chr11:67141792-67141842	HRCEpiC	kidney:	n/a
5	chr11:67141792-67141842	Jurkat	blood:	n/a
6	chr11:67141792-67141842	HMEC	breast:	n/a
7	chr11:67141792-67141842	NHBE	bronchial:	n/a
8	chr11:67141792-67141842	AG09319	gingival:	n/a
9	chr11:67141792-67141842	LNCaP	prostate:	n/a
10	chr11:67141792-67141842	AoSMC	blood vessel:	n/a
11	chr11:67141792-67141842	SAEC	small airway:	n/a
12	chr11:67141792-67141842	U87	brain:	n/a
13	chr11:67141792-67141842	H1-hESC	embryonic stem cell:	embryo
14	chr11:67141792-67141842	AG04450	lung:	fetal
15	chr11:67141792-67141842	SK-N-SH	brain:	n/a
16	chr11:67141792-67141842	HNPCEpiC	eye:	n/a
17	chr11:67141792-67141842	Hela-S3	cervix:	n/a
18	chr11:67141792-67141842	HEK293	kidney:	embryo
19	chr11:67141792-67141842	NHDF-neo	bronchial:	n/a
20	chr11:67141792-67141842	MCF10A-Er-Src	breast:	n/a
21	chr11:67141792-67141842	HL-60	blood:	n/a
22	chr11:67141792-67141842	PrEC	prostate:	n/a
23	chr11:67141792-67141842	HEEpiC	esophagus:	n/a
24	chr11:67141792-67141842	HCT-116	colon:	n/a
25	chr11:67141792-67141842	ovcar-3	ovarian:	n/a
26	chr11:67141792-67141842	PFSK-1	brain:	n/a
27	chr11:67141792-67141842	NB4	blood:	n/a
28	chr11:67141792-67141842	BJ	skin:	n/a
29	chr11:67141792-67141842	Caco-2	colon:	n/a
30	chr11:67141792-67141842	NH-A	brain:	n/a
31	chr11:67141792-67141842	HAEpiC	amniotic membrane:	n/a
32	chr11:67141792-67141842	AG04449	skin:	fetal
33	chr11:67141792-67141842	HCM	heart:	n/a
34	chr11:67141792-67141842	T-47D	breast:	n/a
35	chr11:67141792-67141842	PANC-1	pancreas:	n/a
36	chr11:67141792-67141842	NT2-D1	testis:	n/a
37	chr11:67141792-67141842	GM19239	blood:	n/a
38	chr11:67141792-67141842	GM06990	blood:	n/a
39	chr11:67141792-67141842	MCF-7	breast:	n/a
40	chr11:67141792-67141842	HCPEpiC	choroid plexus:	n/a
41	chr11:67141792-67141842	Hepatocyte	liver:	n/a
42	chr11:67141792-67141842	HRPEpiC	eye:	n/a
43	chr11:67141792-67141842	K562	blood:	n/a
44	chr11:67141792-67141842	A549	lung:	n/a
45	chr11:67141792-67141842	BE2_C	brain:	n/a
46	chr11:67141792-67141842	SK-N-MC	brain:	n/a
47	chr11:67141792-67141842	CMK	blood:	n/a
48	chr11:67141792-67141842	RPTEC	kidney:	n/a
49	chr11:67141792-67141842	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:67141792-67141842	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67140365..67142235-chr11:67187974..67189991,2	K562	blood:
2	chr11:67140165..67142541-chr11:67273740..67276217,2	MCF-7	breast:
3	chr11:66821897..66826528-chr11:67139094..67144065,11	MCF-7	breast:
4	chr11:67031846..67035344-chr11:67139453..67142374,3	K562	blood:
5	chr11:67006828..67010582-chr11:67138867..67142453,4	MCF-7	breast:
6	chr1:110752769..110754407-chr11:67141303..67143426,2	MCF-7	breast:
7	chr11:67053474..67057507-chr11:67138689..67143945,8	MCF-7	breast:
8	chr11:67138872..67142169-chr11:67249496..67254071,4	MCF-7	breast:
9	chr11:67033933..67038277-chr11:67140224..67143646,5	MCF-7	breast:
10	chr11:67124080..67124985-chr11:67141333..67142050,4	K562	blood:
11	chr11:67069872..67072644-chr11:67140515..67142125,2	K562	blood:
12	chr11:67141590..67142463-chr11:111749577..111750345,2	Hela-S3	cervix:
13	chr11:66823034..66824892-chr11:67139520..67142366,3	MCF-7	breast:
14	chr11:67120355..67120891-chr11:67141344..67142247,2	MCF-7	breast:
15	chr11:67140268..67142517-chr20:55839534..55841832,2	MCF-7	breast:
16	chr11:67141172..67143536-chr11:67171363..67173683,2	K562	blood:
17	chr11:67139765..67142051-chr17:57918264..57920706,2	MCF-7	breast:
18	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
19	chr11:67140319..67142184-chr11:67395845..67397635,2	MCF-7	breast:
20	chr11:67124136..67124774-chr11:67141523..67142327,3	MCF-7	breast:
21	chr11:67141684..67144612-chr14:62266117..62268626,2	MCF-7	breast:
22	chr11:67077940..67083214-chr11:67140082..67142904,6	MCF-7	breast:
23	chr11:67140485..67142430-chr11:67273527..67275502,2	K562	blood:
24	chr11:67138430..67143112-chr11:67157518..67161987,7	K562	blood:
25	chr11:67139501..67142119-chr16:3071898..3074181,2	MCF-7	breast:
26	chr11:67070466..67072644-chr11:67139702..67142015,2	K562	blood:
27	chr11:67141166..67142111-chr16:30709540..30710323,2	Hela-S3	cervix:
28	chr11:67139623..67143035-chr11:67167894..67169679,3	K562	blood:
29	chr11:67140815..67142437-chr11:67396749..67399508,2	MCF-7	breast:
30	chr11:67141563..67142093-chr2:37193174..37193824,2	Hela-S3	cervix:
31	chr11:67140774..67143112-chr11:67157579..67159214,2	K562	blood:
32	chr11:67069246..67073295-chr11:67139634..67145393,8	MCF-7	breast:
33	chr11:67140249..67142626-chr11:67380875..67383552,2	MCF-7	breast:
34	chr11:67078342..67081725-chr11:67139517..67143464,5	MCF-7	breast:
35	chr11:67030856..67037366-chr11:67138319..67144892,13	MCF-7	breast:
36	chr11:67116951..67127260-chr11:67135118..67146037,42	K562	blood:
37	chr11:67139414..67143301-chr11:67273275..67276817,6	MCF-7	breast:

Variant related genes	Relation type
CLCF1	TF binding region
ENSG00000256514	TF binding region
CLCF1	CpG island
ENSG00000256514	CpG island
ENSG00000255561	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000137720	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000167799	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000231793	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000116396	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000258529	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000103145	Chromatin interaction
ENSG00000173156	Chromatin interaction
ENSG00000173120	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000115808	Chromatin interaction
ENSG00000131652	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers 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	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
6	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
7	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
8	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS 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 miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
9	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription 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	146 gene(s)	inside rSNPs	diseases
11	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
13	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
14	esv3404685	chr11:67139076-67142024	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
15	esv3323213	chr11:67139601-67142149	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
16	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer 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	154 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67136800-67143600	Bivalent Enhancer	Fetal Thymus	thymus
2	chr11:67139400-67142000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:67139400-67142000	Active TSS	Muscle Satellite Cultured Cells	--
4	chr11:67139600-67142000	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr11:67139600-67142000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:67139600-67142000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:67139600-67142000	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr11:67139600-67142000	Active TSS	NHDF-Ad	bronchial
9	chr11:67139600-67142400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr11:67139800-67142000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:67139800-67142000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr11:67139800-67142000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:67139800-67142000	Active TSS	A549	lung
14	chr11:67139800-67142200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:67140200-67142200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:67140600-67142000	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr11:67140600-67142000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr11:67140600-67142600	Bivalent Enhancer	Fetal Brain Male	brain
19	chr11:67140800-67142000	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr11:67140800-67142000	Flanking Active TSS	Liver	Liver
21	chr11:67140800-67142000	Flanking Active TSS	Colonic Mucosa	Colon
22	chr11:67141000-67142000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:67141000-67142200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:67141000-67142200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
25	chr11:67141000-67142200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr11:67141000-67142600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr11:67141200-67142000	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr11:67141200-67142000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:67141200-67142000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:67141200-67142000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
31	chr11:67141200-67142200	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr11:67141200-67142200	Enhancers	Brain Cingulate Gyrus	brain
33	chr11:67141200-67142200	Flanking Active TSS	Stomach Mucosa	stomach
34	chr11:67141200-67142200	Enhancers	Spleen	Spleen
35	chr11:67141200-67142400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr11:67141400-67142000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:67141400-67142000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
38	chr11:67141400-67142000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:67141400-67142000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr11:67141400-67142000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:67141400-67142000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr11:67141400-67142000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
43	chr11:67141400-67142000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr11:67141400-67142000	Flanking Active TSS	HepG2	liver
45	chr11:67141400-67142000	Flanking Active TSS	HUVEC	blood vessel
46	chr11:67141400-67142200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:67141400-67142200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr11:67141400-67142200	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr11:67141400-67142200	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr11:67141400-67142200	Flanking Active TSS	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links