Variant report

Variant	rs3750122
Chromosome Location	chr7:33168903-33168904
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	MYBL2	chr7:33168513-33169472	HepG2	liver:	n/a	n/a
2	USF1	chr7:33168676-33169371	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr7:33168823-33169163	K562	blood:	n/a	n/a
4	MYC	chr7:33168360-33169515	K562	blood:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
5	POLR2A	chr7:33168512-33169389	HepG2	liver:	n/a	n/a
6	ZNF143	chr7:33168600-33169591	GM12878	blood:	n/a	chr7:33168891-33168909 chr7:33169109-33169127
7	POLR2A	chr7:33168527-33169399	HEK293	kidney:	n/a	n/a
8	MAX	chr7:33168451-33169407	A549	lung:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
9	MAX	chr7:33168671-33169150	K562	blood:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
10	YY1	chr7:33168567-33169417	HepG2	liver:	n/a	chr7:33168891-33168902 chr7:33168839-33168848
11	POLR2A	chr7:33168551-33169607	Gliobla	brain:	n/a	n/a
12	ZNF143	chr7:33168637-33169345	Hela-S3	cervix:	n/a	chr7:33168891-33168909 chr7:33169109-33169127
13	USF1	chr7:33168751-33169377	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:33168551-33169462	GM15510	blood:	n/a	n/a
15	CCNT2	chr7:33168561-33169258	K562	blood:	n/a	chr7:33168839-33168848
16	POLR2A	chr7:33168477-33169461	SK-N-SH	brain:	n/a	n/a
17	MAFK	chr7:33168718-33169259	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr7:33168567-33168981	A549	lung:	n/a	n/a
19	POLR2A	chr7:33168497-33169432	GM12878	blood:	n/a	n/a
20	POLR2A	chr7:33168518-33169460	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr7:33168602-33169350	A549	lung:	n/a	n/a
22	MAX	chr7:33168370-33169462	A549	lung:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
23	CHD2	chr7:33168566-33169229	HepG2	liver:	n/a	chr7:33168837-33168847
24	MAX	chr7:33168515-33169505	SK-N-SH	brain:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
25	USF1	chr7:33168688-33169283	SK-N-SH_RA	brain:	n/a	n/a
26	TCF12	chr7:33168704-33169413	ECC-1	luminal epithelium:	n/a	n/a
27	MXI1	chr7:33168713-33169291	K562	blood:	n/a	n/a
28	SIX5	chr7:33168883-33169334	K562	blood:	n/a	n/a
29	NFYB	chr7:33168817-33168944	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr7:33168399-33169490	HUVEC	blood vessel:	n/a	n/a
31	PAX5	chr7:33168569-33169045	GM12892	blood:	n/a	n/a
32	PAX5	chr7:33168771-33169315	GM12878	blood:	n/a	n/a
33	CREB1	chr7:33168532-33169522	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:33168391-33169461	SK-N-MC	brain:	n/a	n/a
35	RUNX3	chr7:33168574-33169386	GM12878	blood:	n/a	n/a
36	USF1	chr7:33168699-33169311	A549	lung:	n/a	n/a
37	POLR2A	chr7:33168479-33169519	MCF-7	breast:	n/a	n/a
38	USF1	chr7:33168608-33169194	A549	lung:	n/a	n/a
39	POLR2A	chr7:33168590-33169414	GM12878	blood:	n/a	n/a
40	CTCF	chr7:33168820-33168970	AG09319	gingival:	n/a	n/a
41	CHD2	chr7:33168610-33169651	GM12878	blood:	n/a	chr7:33168837-33168847
42	MAX	chr7:33168406-33169505	MCF-7	breast:	n/a	chr7:33168891-33168901 chr7:33168840-33168850
43	USF1	chr7:33168706-33169267	A549	lung:	n/a	n/a
44	EP300	chr7:33168800-33169245	GM12878	blood:	n/a	n/a
45	TCF7L2	chr7:33168335-33169283	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:33168469-33169492	U87	brain:	n/a	n/a
47	YY1	chr7:33168891-33169349	GM12892	blood:	n/a	chr7:33168891-33168902
48	MXI1	chr7:33168372-33169502	GM12878	blood:	n/a	n/a
49	RCOR1	chr7:33168589-33169604	K562	blood:	n/a	n/a
50	USF1	chr7:33168660-33169350	SK-N-SH_RA	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
2	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:

Variant related genes	Relation type
BBS9	TF binding region
ENSG00000228015	TF binding region
ENSG00000164610	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1019301	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10269945	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274959	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10486523	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10486525	0.82[ASN][1000 genomes]
rs1362370	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16879114	0.82[EUR][1000 genomes]
rs17169807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17170099	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170104	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170105	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17170120	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17170131	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17170138	0.82[ASN][1000 genomes]
rs17170140	0.82[ASN][1000 genomes]
rs17170143	0.82[ASN][1000 genomes]
rs17170155	0.82[ASN][1000 genomes]
rs17170167	0.80[ASN][1000 genomes]
rs17170169	0.80[ASN][1000 genomes]
rs17170173	0.80[ASN][1000 genomes]
rs17170178	0.80[ASN][1000 genomes]
rs1833176	0.80[ASN][1000 genomes]
rs2392229	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34950347	0.82[ASN][1000 genomes]
rs3828996	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4538777	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4628178	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55829345	0.87[EUR][1000 genomes]
rs55847945	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55865959	0.82[ASN][1000 genomes]
rs55924837	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55934422	0.84[AMR][1000 genomes]
rs56195645	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56205706	0.84[AMR][1000 genomes]
rs56343904	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs58550767	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59075362	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs59446325	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60146993	0.82[EUR][1000 genomes]
rs60268357	0.82[ASN][1000 genomes]
rs60491621	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6943198	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6944559	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6952244	0.82[ASN][1000 genomes]
rs6969284	0.82[ASN][1000 genomes]
rs6973114	0.82[EUR][1000 genomes]
rs6973552	0.82[ASN][1000 genomes]
rs72496118	0.84[AMR][1000 genomes]
rs73307386	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73307398	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73307399	0.80[EUR][1000 genomes]
rs73307400	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73307585	0.82[AFR][1000 genomes]
rs73307589	0.85[AFR][1000 genomes]
rs73307592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73309308	0.82[ASN][1000 genomes]
rs73309310	0.82[ASN][1000 genomes]
rs73309316	0.82[ASN][1000 genomes]
rs73309318	0.82[ASN][1000 genomes]
rs73309324	0.82[ASN][1000 genomes]
rs73309326	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73309328	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73309405	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73309423	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73313121	0.80[ASN][1000 genomes]
rs73313134	0.80[ASN][1000 genomes]
rs73313138	0.80[ASN][1000 genomes]
rs73313148	0.80[AMR][1000 genomes]
rs73317492	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73319406	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73319407	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73319408	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73688093	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73689881	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7459365	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781504	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7793667	0.82[ASN][1000 genomes]
rs7795704	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7796922	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7798118	0.82[ASN][1000 genomes]
rs7799346	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7808472	0.82[ASN][1000 genomes]
rs7809235	0.82[EUR][1000 genomes]
rs7809366	0.82[EUR][1000 genomes]
rs9791555	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9791901	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029220	chr7:32921484-33262190	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised 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
2	nsv830942	chr7:33048075-33246735	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv508450	chr7:33123335-33184848	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1033502	chr7:33124005-33185470	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1025361	chr7:33125663-33185470	Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv869720	chr7:33127192-33193580	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1026615	chr7:33128234-33185470	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1020741	chr7:33130675-33185470	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1027807	chr7:33130675-33190591	Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv2761318	chr7:33130687-33185482	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv464422	chr7:33131729-33187279	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv606606	chr7:33131729-33187279	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv606607	chr7:33131729-33192502	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv464423	chr7:33131729-33192800	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv606608	chr7:33131729-33192800	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv520406	chr7:33131729-33192837	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
17	nsv606609	chr7:33131729-33196354	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
18	nsv1030007	chr7:33132814-33185470	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv1028637	chr7:33133742-33185470	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv830943	chr7:33167106-33352759	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33168000-33169600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:33168000-33169800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:33168000-33170000	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr7:33168000-33170200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr7:33168200-33169200	Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr7:33168200-33169400	Active TSS	Primary hematopoietic stem cells	blood
7	chr7:33168200-33169400	Active TSS	NHEK	skin
8	chr7:33168200-33169600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:33168200-33169600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:33168200-33169600	Active TSS	Brain Substantia Nigra	brain
11	chr7:33168200-33169600	Active TSS	Duodenum Mucosa	Duodenum
12	chr7:33168200-33169600	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr7:33168200-33169600	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr7:33168200-33169800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr7:33168200-33169800	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr7:33168200-33169800	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr7:33168200-33169800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:33168200-33169800	Active TSS	Muscle Satellite Cultured Cells	--
19	chr7:33168200-33169800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:33168200-33169800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:33168200-33169800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:33168200-33169800	Active TSS	Colon Smooth Muscle	Colon
23	chr7:33168200-33169800	Active TSS	Fetal Brain Female	brain
24	chr7:33168200-33169800	Active TSS	Fetal Kidney	kidney
25	chr7:33168200-33169800	Active TSS	Placenta Amnion	Placenta Amnion
26	chr7:33168200-33169800	Active TSS	Stomach Smooth Muscle	stomach
27	chr7:33168200-33169800	Active TSS	GM12878-XiMat	blood
28	chr7:33168200-33170000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:33168200-33170000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:33168200-33170000	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr7:33168200-33170000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:33168200-33170000	Active TSS	Brain Cingulate Gyrus	brain
33	chr7:33168200-33170000	Active TSS	Fetal Intestine Large	intestine
34	chr7:33168200-33170200	Active TSS	H1 Cell Line	embryonic stem cell
35	chr7:33168200-33170200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:33168200-33170200	Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr7:33168200-33170200	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr7:33168200-33170200	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr7:33168200-33170600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:33168400-33169200	Active TSS	Primary monocytes fromperipheralblood	blood
41	chr7:33168400-33169200	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr7:33168400-33169400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:33168400-33169400	Active TSS	Primary B cells from peripheral blood	blood
44	chr7:33168400-33169400	Active TSS	Primary T cells fromperipheralblood	blood
45	chr7:33168400-33169400	Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr7:33168400-33169400	Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr7:33168400-33169400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:33168400-33169400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
49	chr7:33168400-33169600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:33168400-33169600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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