Variant report

Variant	rs4718277
Chromosome Location	chr7:65235405-65235406
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	YY1	chr7:65235376-65236241	GM12892	blood:	n/a	n/a
2	TCF12	chr7:65235305-65236092	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:65235289-65236583	SK-N-MC	brain:	n/a	n/a
4	BCL11A	chr7:65235220-65235406	GM12878	blood:	n/a	n/a
5	TAF1	chr7:65235220-65236243	H1-hESC	embryonic stem cell:	n/a	n/a
6	POU2F2	chr7:65235292-65236277	GM12891	blood:	n/a	n/a
7	NR2F2	chr7:65235053-65236534	K562	blood:	n/a	n/a
8	TAF1	chr7:65235250-65236079	HepG2	liver:	n/a	n/a
9	POLR2A	chr7:65235405-65236558	K562	blood:	n/a	n/a
10	POLR2A	chr7:65235357-65236570	MCF-7	breast:	n/a	n/a
11	POLR2A	chr7:65235293-65236214	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:65235144-65236401	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZNF143	chr7:65235403-65235919	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:65235339-65236789	GM12878	blood:	n/a	n/a
15	POLR2A	chr7:65234863-65236998	HepG2	liver:	n/a	n/a
16	SIN3AK20	chr7:65235383-65235812	HepG2	liver:	n/a	n/a
17	POLR2A	chr7:65235243-65236620	GM12892	blood:	n/a	n/a
18	POLR2A	chr7:65235316-65236704	K562	blood:	n/a	n/a
19	POLR2A	chr7:65235357-65236222	Gliobla	brain:	n/a	n/a
20	PML	chr7:65235264-65236282	GM12878	blood:	n/a	n/a
21	EBF1	chr7:65235287-65235727	GM12878	blood:	n/a	n/a
22	TCF12	chr7:65235355-65235899	A549	lung:	n/a	n/a
23	TCF12	chr7:65235316-65235707	GM12878	blood:	n/a	n/a
24	GABPA	chr7:65235214-65235711	K562	blood:	n/a	n/a
25	SP1	chr7:65235398-65236173	GM12878	blood:	n/a	chr7:65235812-65235824 chr7:65235812-65235824 chr7:65235814-65235823 chr7:65235812-65235823 chr7:65235861-65235870
26	POLR2A	chr7:65235389-65236208	HepG2	liver:	n/a	n/a
27	NRF1	chr7:65235280-65236128	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr7:65235320-65236604	GM12891	blood:	n/a	n/a
29	MYC	chr7:65235349-65235881	MCF-7	breast:	n/a	n/a
30	POLR2A	chr7:65235391-65236277	Hela-S3	cervix:	n/a	n/a
31	TCF3	chr7:65235259-65235993	GM12878	blood:	n/a	n/a
32	CBX3	chr7:65235258-65236679	K562	blood:	n/a	n/a
33	POLR2A	chr7:65235329-65236266	U87	brain:	n/a	n/a
34	POLR2A	chr7:65235321-65236313	Hela-S3	cervix:	n/a	n/a
35	PAX5	chr7:65235379-65235788	GM12892	blood:	n/a	n/a
36	POLR2A	chr7:65235373-65236116	HepG2	liver:	n/a	n/a
37	HEY1	chr7:65235356-65236589	K562	blood:	n/a	chr7:65235851-65235860 chr7:65235849-65235858
38	POLR2A	chr7:65235319-65236233	H1-hESC	embryonic stem cell:	n/a	n/a
39	IRF4	chr7:65235330-65236203	GM12878	blood:	n/a	n/a
40	POLR2A	chr7:65235291-65236371	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr7:65235379-65236230	PANC-1	pancreas:	n/a	n/a
42	MYBL2	chr7:65235402-65236243	HepG2	liver:	n/a	n/a
43	POLR2A	chr7:65235340-65236263	ProgFib	skin:	n/a	n/a
44	PAX5	chr7:65235327-65236071	GM12878	blood:	n/a	chr7:65235954-65235963
45	JUND	chr7:65235386-65236569	SK-N-SH	brain:	n/a	chr7:65235850-65235859
46	POLR2A	chr7:65235402-65236035	A549	lung:	n/a	n/a
47	POLR2A	chr7:65235293-65236594	GM12892	blood:	n/a	n/a
48	PAX5	chr7:65235304-65236226	GM12878	blood:	n/a	chr7:65235954-65235963
49	POLR2A	chr7:65235203-65236726	GM12878	blood:	n/a	n/a
50	ELF1	chr7:65235382-65236230	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:64540231..64542866-chr7:65234211..65237009,2	MCF-7	breast:
2	chr7:64541401..64541976-chr7:65235201..65235732,3	MCF-7	breast:
3	chr7:65213884..65218183-chr7:65233667..65237121,4	K562	blood:
4	chr7:64541160..64542217-chr7:65235379..65236226,3	HCT-116	colon:
5	chr7:64541143..64541896-chr7:65235210..65235720,2	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000224316	TF binding region
ENSG00000228409	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10247899	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10250008	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10279930	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1061361	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11538349	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs11971971	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap]
rs12698508	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs12698509	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs13235246	0.86[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap]
rs13236109	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap]
rs13239979	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs1799103	0.81[ASN][1000 genomes]
rs1851840	0.91[CEU][hapmap]
rs2272185	0.89[ASN][1000 genomes]
rs2419433	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2419434	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2690405	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2900904	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34136756	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs34193460	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs34529418	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap]
rs34637256	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs34933526	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs35310401	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs35391607	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs35480979	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs35735127	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap]
rs3734912	0.92[ASN][1000 genomes]
rs3813708	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs4718267	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718269	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718270	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718273	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4718274	0.88[AMR][1000 genomes]
rs4718276	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460260	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460261	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6949812	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs6970243	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7781958	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7789975	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7792846	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7793966	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7794661	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7795242	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs937108	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs9768509	1.00[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517778	chr7:64462326-65326821	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv429767	chr7:64473713-65415647	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv917231	chr7:64478253-65300317	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv1029796	chr7:64494934-65302696	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	esv3339156	chr7:64510176-65349050	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	esv2759534	chr7:64551274-65373851	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv427788	chr7:64551274-65390424	Weak transcription Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
8	esv2764020	chr7:64594065-65351820	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv1018447	chr7:64609892-65308719	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv538897	chr7:64609892-65308719	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv1029942	chr7:64679680-65371565	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
12	nsv538903	chr7:64679680-65371565	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
13	nsv1019667	chr7:64679680-65380603	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
14	esv2757227	chr7:64694241-65373851	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
15	nsv1025207	chr7:65092426-65339879	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
16	nsv1033400	chr7:65092426-65339879	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
17	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv1020622	chr7:65161364-65339879	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4718277	VKORC1L1	cis	Whole Blood	GTEx
rs4718277	GUSB	cis	Whole Blood	GTEx
rs4718277	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs4718277	RP4-756H11.3	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65234200-65236600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:65234200-65236600	Active TSS	Hela-S3	cervix
3	chr7:65234400-65236000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:65234600-65236200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:65234600-65236200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:65234600-65236400	Active TSS	Liver	Liver
7	chr7:65234800-65236000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:65234800-65236200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:65234800-65236400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr7:65234800-65236400	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr7:65234800-65236600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:65235000-65236000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
13	chr7:65235000-65236200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:65235000-65236200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:65235000-65236200	Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr7:65235000-65236200	Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr7:65235000-65236200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:65235000-65236200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:65235000-65236200	Active TSS	Fetal Brain Female	brain
20	chr7:65235000-65236200	Active TSS	Fetal Intestine Small	intestine
21	chr7:65235000-65236200	Active TSS	Fetal Stomach	stomach
22	chr7:65235000-65236200	Active TSS	Right Ventricle	heart
23	chr7:65235000-65236400	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr7:65235000-65236400	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr7:65235000-65236400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:65235000-65236400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:65235000-65236400	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr7:65235000-65236600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:65235000-65236600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:65235200-65235800	Active TSS	Primary hematopoietic stem cells	blood
31	chr7:65235200-65235800	Active TSS	Sigmoid Colon	Sigmoid Colon
32	chr7:65235200-65236000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:65235200-65236000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:65235200-65236000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:65235200-65236000	Active TSS	Primary B cells from peripheral blood	blood
36	chr7:65235200-65236000	Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr7:65235200-65236000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr7:65235200-65236000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:65235200-65236000	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:65235200-65236000	Active TSS	Brain Cingulate Gyrus	brain
41	chr7:65235200-65236000	Active TSS	Fetal Muscle Leg	muscle
42	chr7:65235200-65236000	Active TSS	Placenta	Placenta
43	chr7:65235200-65236000	Active TSS	Placenta Amnion	Placenta Amnion
44	chr7:65235200-65236000	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr7:65235200-65236000	Active TSS	Small Intestine	intestine
46	chr7:65235200-65236000	Active TSS	NH-A	brain
47	chr7:65235200-65236200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:65235200-65236200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:65235200-65236200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:65235200-65236200	Active TSS	H9 Cell Line	embryonic stem cell

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