Variant report

Variant	rs11687113
Chromosome Location	chr2:96658588-96658589
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	CTCF	chr2:96658520-96658670	AG09309	skin:	n/a	n/a
2	CTCF	chr2:96658520-96658670	HCPEpiC	choroid plexus:	n/a	n/a
3	SP1	chr2:96657341-96658972	GM12878	blood:	n/a	chr2:96657731-96657745 chr2:96657736-96657745 chr2:96657735-96657745 chr2:96657735-96657744 chr2:96657734-96657746 chr2:96657734-96657746
4	SPI1	chr2:96658438-96658829	GM12878	blood:	n/a	n/a
5	SIN3AK20	chr2:96658513-96658840	HepG2	liver:	n/a	n/a
6	RAD21	chr2:96658365-96658821	HCT-116	colon:	n/a	chr2:96658685-96658704 chr2:96658687-96658694 chr2:96658753-96658772
7	CTCF	chr2:96658581-96658844	GM20000	blood:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
8	FOXP2	chr2:96658549-96658874	SK-N-MC	brain:	n/a	n/a
9	CTCF	chr2:96658540-96658690	NHDF-neo	bronchial:	n/a	n/a
10	SP1	chr2:96658505-96658979	HepG2	liver:	n/a	n/a
11	CTCF	chr2:96658565-96658896	GM10266	blood:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
12	RAD21	chr2:96658583-96658849	A549	lung:	n/a	chr2:96658685-96658704 chr2:96658687-96658694 chr2:96658753-96658772
13	EP300	chr2:96658527-96658757	GM12878	blood:	n/a	n/a
14	POLR2A	chr2:96658466-96658657	MCF10A-Er-Src	breast:	n/a	n/a
15	CTCF	chr2:96658568-96658884	LNCaP	prostate:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
16	CTCF	chr2:96658411-96658824	HCT-116	colon:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
17	MYBL2	chr2:96657393-96658961	HepG2	liver:	n/a	chr2:96657778-96657792
18	MAX	chr2:96658231-96658649	A549	lung:	n/a	chr2:96658301-96658309
19	CTCF	chr2:96658520-96658670	Caco-2	colon:	n/a	n/a
20	CTCF	chr2:96658499-96658934	H1-hESC	embryonic stem cell:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
21	SP1	chr2:96658565-96658905	GM12878	blood:	n/a	n/a
22	CTCF	chr2:96658540-96658690	GM12864	blood:	n/a	n/a
23	SIN3A	chr2:96658392-96658819	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr2:96658540-96658690	HFF	foreskin:	n/a	n/a
25	RAD21	chr2:96658513-96658879	HepG2	liver:	n/a	chr2:96658685-96658704 chr2:96658687-96658694 chr2:96658753-96658772
26	IRF4	chr2:96657365-96659011	GM12878	blood:	n/a	n/a
27	IRF4	chr2:96658259-96658926	GM12878	blood:	n/a	n/a
28	POLR2A	chr2:96657431-96658742	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr2:96658520-96658670	NHLF	lung:	n/a	n/a
30	POLR2A	chr2:96657046-96658606	GM12878	blood:	n/a	n/a
31	CTCF	chr2:96658520-96658670	GM12865	blood:	n/a	n/a
32	CTCF	chr2:96658500-96658650	A549	lung:	n/a	n/a
33	CTCF	chr2:96658575-96658846	HepG2	liver:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
34	TAF1	chr2:96657315-96658842	H1-hESC	embryonic stem cell:	n/a	n/a
35	TEAD4	chr2:96658548-96658977	H1-hESC	embryonic stem cell:	n/a	n/a
36	TCF3	chr2:96657443-96658689	GM12878	blood:	n/a	chr2:96658363-96658376
37	CTCF	chr2:96658540-96658690	GM12872	blood:	n/a	n/a
38	REST	chr2:96658383-96658782	A549	lung:	n/a	n/a
39	TAF1	chr2:96657382-96658674	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr2:96658538-96658703	H1-neurons	neurons:	n/a	n/a
41	CTCF	chr2:96658511-96658849	MCF-7	breast:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
42	CTCF	chr2:96658540-96658690	MCF-7	breast:	n/a	n/a
43	POLR2A	chr2:96657095-96658969	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:96658533-96658870	HUVEC	blood vessel:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
45	TBP	chr2:96658569-96658805	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr2:96658556-96658860	GM13976	blood:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
47	USF1	chr2:96658462-96658921	A549	lung:	n/a	n/a
48	ARID3A	chr2:96658478-96658839	HepG2	liver:	n/a	n/a
49	HEY1	chr2:96657267-96658946	HepG2	liver:	n/a	chr2:96658458-96658473 chr2:96658194-96658209 chr2:96658478-96658487 chr2:96658146-96658161 chr2:96657728-96657743 chr2:96657730-96657745
50	CTCF	chr2:96658560-96658710	BJ	skin:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658686-96658707

No.	Distal block	Cell Line	Cell type
1	chr2:96658288..96659130-chr2:96839638..96840848,4	MCF-7	breast:
2	chr2:96658361..96659117-chr2:98208510..98209019,2	MCF-7	breast:
3	chr2:96656872..96660081-chr2:96874473..96876452,3	MCF-7	breast:
4	chr2:96656483..96658831-chr2:96781728..96784486,2	K562	blood:

Variant related genes	Relation type
ANKRD36C	TF binding region
ENSG00000084090	Chromatin interaction
ENSG00000222040	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11680950	0.82[GIH][hapmap]
rs11683523	0.91[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap]
rs1168965	0.89[GIH][hapmap]
rs1168968	0.92[GIH][hapmap]
rs1168974	0.92[GIH][hapmap]
rs1168976	0.92[GIH][hapmap]
rs11689832	0.91[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap]
rs11695514	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap]
rs2229169	0.85[CEU][hapmap]
rs2312955	0.92[GIH][hapmap]
rs2438972	0.82[CEU][hapmap]
rs2438978	0.90[CEU][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2462774	0.82[CEU][hapmap]
rs2462776	0.82[ASN][1000 genomes]
rs2579515	0.94[ASN][1000 genomes]
rs2579517	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2579519	0.82[CEU][hapmap];0.89[GIH][hapmap]
rs2692893	0.86[CEU][hapmap];0.86[CHD][hapmap];0.97[GIH][hapmap];0.84[MEX][hapmap]
rs2692894	0.92[GIH][hapmap]
rs2692954	0.93[ASN][1000 genomes]
rs2918816	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2918929	0.88[ASN][1000 genomes]
rs2969475	0.93[ASN][1000 genomes]
rs2969477	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4144055	0.87[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4426564	0.92[GIH][hapmap]
rs4527246	0.82[CEU][hapmap]
rs4907226	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4907288	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs62155508	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62155510	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62155511	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6740563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72492201	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7423942	0.86[EUR][1000 genomes]
rs893173	0.80[GIH][hapmap]

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	esv3416818	chr2:96072529-96680708	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv874660	chr2:96091132-96669134	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv516044	chr2:96150959-96683378	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv1003371	chr2:96326106-96684876	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv874666	chr2:96370571-96691125	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv961832	chr2:96453677-96671971	Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv834304	chr2:96493545-96667472	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1004486	chr2:96544604-96684876	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv874669	chr2:96547820-96691125	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv818073	chr2:96554851-96683378	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	esv1840487	chr2:96582807-96836512	Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
12	nsv870250	chr2:96610946-96739308	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	esv1838669	chr2:96613136-96674509	Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	esv1839005	chr2:96613136-96674509	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	esv1836246	chr2:96622689-96674509	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	esv1837811	chr2:96622689-96730375	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
17	nsv874670	chr2:96637870-96693357	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
18	nsv874671	chr2:96637870-96727850	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv874672	chr2:96637870-96809331	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
20	nsv874673	chr2:96647856-96825363	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
21	nsv874674	chr2:96651163-96741944	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs11687113	AC008268.2	cis	Nerve Tibial	GTEx
rs11687113	ZNF514	cis	parietal	SCAN
rs11687113	ADRA2B	cis	Thyroid	GTEx
rs11687113	FER1L5	cis	cerebellum	SCAN
rs11687113	MGAT4A	cis	parietal	SCAN
rs11687113	ZNF514	cis	cerebellum	SCAN
rs11687113	FAHD2CP	cis	lung	GTEx
rs11687113	AC008268.2	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96655800-96658600	Active TSS	Fetal Brain Female	brain
2	chr2:96655800-96658600	Active TSS	K562	blood
3	chr2:96656400-96658600	Active TSS	NH-A	brain
4	chr2:96656400-96658800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:96656400-96658800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:96656400-96658800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:96656400-96658800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:96656400-96658800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:96656400-96658800	Active TSS	Brain Germinal Matrix	brain
10	chr2:96656400-96658800	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr2:96656600-96658600	Active TSS	H9 Cell Line	embryonic stem cell
12	chr2:96656600-96658600	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr2:96656600-96658600	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr2:96656600-96658600	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr2:96656600-96658600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:96656600-96658600	Active TSS	Brain Anterior Caudate	brain
17	chr2:96656600-96658600	Active TSS	Fetal Intestine Small	intestine
18	chr2:96656600-96658600	Active TSS	Fetal Stomach	stomach
19	chr2:96656600-96658600	Active TSS	Fetal Thymus	thymus
20	chr2:96656600-96658600	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr2:96656600-96658600	Active TSS	Right Atrium	heart
22	chr2:96656600-96658800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:96656600-96658800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:96656600-96658800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:96656600-96658800	Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr2:96656600-96658800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:96656600-96658800	Active TSS	Duodenum Mucosa	Duodenum
28	chr2:96656600-96658800	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr2:96656600-96658800	Active TSS	A549	lung
30	chr2:96656600-96658800	Active TSS	Dnd41	blood
31	chr2:96656600-96658800	Active TSS	Monocytes-CD14+_RO01746	blood
32	chr2:96656600-96658800	Active TSS	NHDF-Ad	bronchial
33	chr2:96656800-96658600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:96656800-96658600	Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr2:96656800-96658600	Active TSS	Brain Cingulate Gyrus	brain
36	chr2:96656800-96658600	Active TSS	Fetal Muscle Leg	muscle
37	chr2:96656800-96658800	Active TSS	H1 Cell Line	embryonic stem cell
38	chr2:96656800-96658800	Active TSS	Thymus	Thymus
39	chr2:96657000-96658600	Active TSS	Esophagus	oesophagus
40	chr2:96657000-96658600	Active TSS	Psoas Muscle	Psoas
41	chr2:96657000-96658600	Active TSS	Right Ventricle	heart
42	chr2:96657200-96658600	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr2:96657200-96658600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr2:96657200-96658600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:96657200-96658600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:96657200-96658600	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr2:96657200-96658600	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr2:96657200-96658600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr2:96657200-96658600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:96657200-96658600	Active TSS	Primary B cells from peripheral blood	blood

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