Variant report

Variant	rs536552704
Chromosome Location	chr12:57916614-57916615
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	JUND	chr12:57915962-57916855	A549	lung:	n/a	chr12:57916792-57916800 chr12:57916131-57916140 chr12:57916342-57916351 chr12:57916346-57916355
2	EGR1	chr12:57916579-57916806	GM12878	blood:	n/a	chr12:57916726-57916739 chr12:57916725-57916740 chr12:57916621-57916630 chr12:57916763-57916773 chr12:57916731-57916746
3	E2F4	chr12:57915940-57916794	K562	blood:	n/a	chr12:57916768-57916778 chr12:57916654-57916664 chr12:57916651-57916661 chr12:57916621-57916630
4	POLR2A	chr12:57915757-57916804	GM12878	blood:	n/a	n/a
5	POLR2A	chr12:57915733-57918696	ECC-1	luminal epithelium:	n/a	n/a
6	MAX	chr12:57915284-57916825	HepG2	liver:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
7	POLR2A	chr12:57915282-57917210	GM19099	blood:	n/a	n/a
8	SMARCB1	chr12:57915936-57917381	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr12:57915317-57916843	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:57915750-57916775	GM12878	blood:	n/a	chr12:57916650-57916666 chr12:57916653-57916669 chr12:57916649-57916665
11	MAX	chr12:57915577-57916838	ECC-1	luminal epithelium:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
12	EP300	chr12:57916062-57916812	H1-hESC	embryonic stem cell:	n/a	chr12:57916652-57916661
13	POLR2A	chr12:57916055-57916839	A549	lung:	n/a	n/a
14	TBL1XR1	chr12:57915372-57916761	K562	blood:	n/a	n/a
15	RELA	chr12:57915831-57916721	GM10847	blood:	n/a	n/a
16	YY1	chr12:57916551-57916765	A549	lung:	n/a	chr12:57916650-57916659 chr12:57916653-57916667 chr12:57916598-57916609 chr12:57916657-57916668 chr12:57916650-57916664
17	TAF1	chr12:57915799-57916879	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr12:57915393-57917444	GM19193	blood:	n/a	n/a
19	MAX	chr12:57915660-57917188	H1-hESC	embryonic stem cell:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
20	POLR2A	chr12:57913349-57917243	Raji	blood:	n/a	n/a
21	ZNF143	chr12:57915727-57916819	GM12878	blood:	n/a	chr12:57916573-57916588 chr12:57915803-57915818 chr12:57916572-57916591
22	YY1	chr12:57916518-57916766	K562	blood:	n/a	chr12:57916650-57916659 chr12:57916653-57916667 chr12:57916598-57916609 chr12:57916657-57916668 chr12:57916650-57916664
23	JUND	chr12:57916597-57916784	H1-hESC	embryonic stem cell:	n/a	n/a
24	HMGN3	chr12:57916010-57917073	K562	blood:	n/a	n/a
25	CHD2	chr12:57915503-57917183	GM12878	blood:	n/a	n/a
26	HCFC1	chr12:57915227-57917771	Hela-S3	cervix:	n/a	n/a
27	EP300	chr12:57916085-57916734	T-47D	breast:	n/a	chr12:57916652-57916661
28	POLR2A	chr12:57912918-57917367	GM12878	blood:	n/a	n/a
29	POLR2A	chr12:57915483-57918252	Hela-S3	cervix:	n/a	n/a
30	NR2F2	chr12:57915162-57916655	K562	blood:	n/a	chr12:57916076-57916091
31	TAF1	chr12:57916549-57916864	K562	blood:	n/a	n/a
32	POLR2A	chr12:57915371-57916774	GM12891	blood:	n/a	n/a
33	MXI1	chr12:57912772-57916808	IMR90	lung:	n/a	n/a
34	REST	chr12:57915218-57917582	H1-neurons	neurons:	n/a	chr12:57916449-57916458 chr12:57915324-57915338 chr12:57916602-57916615
35	POLR2A	chr12:57916566-57916781	H1-hESC	embryonic stem cell:	n/a	n/a
36	TBL1XR1	chr12:57915371-57916747	K562	blood:	n/a	n/a
37	POLR2A	chr12:57915757-57916806	SK-N-SH	brain:	n/a	n/a
38	E2F6	chr12:57916378-57916621	K562	blood:	n/a	n/a
39	RUNX3	chr12:57915590-57916620	GM12878	blood:	n/a	n/a
40	EGR1	chr12:57916330-57916853	GM12878	blood:	n/a	chr12:57916726-57916739 chr12:57916543-57916557 chr12:57916725-57916740 chr12:57916621-57916630 chr12:57916763-57916773 chr12:57916731-57916746 chr12:57916342-57916352 chr12:57916338-57916348
41	RELA	chr12:57915802-57916688	GM19099	blood:	n/a	n/a
42	HEY1	chr12:57916555-57916737	HepG2	liver:	n/a	chr12:57916654-57916669
43	ELF1	chr12:57916548-57916810	HepG2	liver:	n/a	chr12:57916651-57916663 chr12:57916768-57916780 chr12:57916656-57916665 chr12:57916650-57916659
44	POLR2A	chr12:57915730-57916848	ECC-1	luminal epithelium:	n/a	n/a
45	ELF1	chr12:57916515-57916772	HepG2	liver:	n/a	chr12:57916651-57916663 chr12:57916656-57916665 chr12:57916650-57916659
46	MAZ	chr12:57915727-57917823	GM12878	blood:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
47	POLR2A	chr12:57916510-57916827	A549	lung:	n/a	n/a
48	POLR2A	chr12:57911713-57919299	SK-N-MC	brain:	n/a	n/a
49	POLR2A	chr12:57916535-57916793	HepG2	liver:	n/a	n/a
50	POLR2A	chr12:57916367-57916809	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57916571-57916621	GM19239	blood:	n/a
2	chr12:57916571-57916621	AG04449	skin:	fetal
3	chr12:57916571-57916621	HNPCEpiC	eye:	n/a
4	chr12:57916571-57916621	GM12892	blood:	n/a
5	chr12:57916571-57916621	SK-N-SH	brain:	n/a
6	chr12:57916571-57916621	Hela-S3	cervix:	n/a
7	chr12:57916571-57916621	IMR90	lung:	fetal
8	chr12:57916571-57916621	SAEC	small airway:	n/a
9	chr12:57916571-57916621	AG09319	gingival:	n/a
10	chr12:57916571-57916621	AG04450	lung:	fetal
11	chr12:57916571-57916621	HepG2	liver:	n/a
12	chr12:57916571-57916621	HCPEpiC	choroid plexus:	n/a
13	chr12:57916571-57916621	HCT-116	colon:	n/a
14	chr12:57916571-57916621	GM12878	blood:	n/a
15	chr12:57916571-57916621	AG10803	skin:	n/a
16	chr12:57916571-57916621	ovcar-3	ovarian:	n/a
17	chr12:57916571-57916621	ECC-1	luminal epithelium:	n/a
18	chr12:57916571-57916621	ProgFib	skin:	n/a
19	chr12:57916571-57916621	NT2-D1	testis:	n/a
20	chr12:57916571-57916621	LNCaP	prostate:	n/a
21	chr12:57916571-57916621	HCM	heart:	n/a
22	chr12:57916571-57916621	PANC-1	pancreas:	n/a
23	chr12:57916571-57916621	GM12891	blood:	n/a
24	chr12:57916571-57916621	PrEC	prostate:	n/a
25	chr12:57916571-57916621	BJ	skin:	n/a
26	chr12:57916571-57916621	HRE	kidney:	n/a
27	chr12:57916571-57916621	GM06990	blood:	n/a
28	chr12:57916571-57916621	T-47D	breast:	n/a
29	chr12:57916571-57916621	HEEpiC	esophagus:	n/a
30	chr12:57916571-57916621	Hepatocyte	liver:	n/a
31	chr12:57916571-57916621	Jurkat	blood:	n/a
32	chr12:57916571-57916621	AG09309	skin:	n/a
33	chr12:57916571-57916621	HMEC	breast:	n/a
34	chr12:57916571-57916621	HIPEpiC	eye:	n/a
35	chr12:57916571-57916621	HRCEpiC	kidney:	n/a
36	chr12:57916571-57916621	NHBE	bronchial:	n/a
37	chr12:57916571-57916621	SK-N-SH_RA	brain:	n/a
38	chr12:57916571-57916621	SKMC	muscle:	n/a
39	chr12:57916571-57916621	HAEpiC	amniotic membrane:	n/a
40	chr12:57916571-57916621	HL-60	blood:	n/a
41	chr12:57916571-57916621	AoSMC	blood vessel:	n/a
42	chr12:57916571-57916621	HEK293	kidney:	embryo
43	chr12:57916571-57916621	SK-N-MC	brain:	n/a
44	chr12:57916571-57916621	Caco-2	colon:	n/a
45	chr12:57916571-57916621	HCF	heart:	n/a
46	chr12:57916571-57916621	NB4	blood:	n/a
47	chr12:57916571-57916621	RPTEC	kidney:	n/a
48	chr12:57916571-57916621	NHDF-neo	bronchial:	n/a
49	chr12:57916571-57916621	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:57916571-57916621	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:57117159..57119489-chr12:57914533..57916753,2	K562	blood:
2	chr12:57879207..57888227-chr12:57906247..57918451,36	K562	blood:
3	chr12:57915553..57917499-chr12:58144787..58147876,3	K562	blood:
4	chr12:57915782..57916713-chr12:58026905..58027434,2	MCF-7	breast:
5	chr12:57915482..57918597-chr12:58119014..58121092,3	MCF-7	breast:
6	chr12:57914556..57917935-chr12:58138142..58139921,3	K562	blood:
7	chr12:57916512..57918954-chr12:58138893..58140769,2	MCF-7	breast:
8	chr12:57915284..57917737-chr12:58135302..58137824,2	K562	blood:
9	chr12:57890108..57896575-chr12:57912675..57917509,9	MCF-7	breast:
10	chr12:57852034..57858739-chr12:57911478..57917144,8	MCF-7	breast:
11	chr12:57822673..57825673-chr12:57914537..57916745,4	K562	blood:
12	chr12:57916469..57918452-chr12:58024223..58025919,2	K562	blood:
13	chr12:57880552..57883318-chr12:57915762..57917586,2	MCF-7	breast:
14	chr12:57913857..57916876-chr12:58140485..58143986,3	K562	blood:
15	chr12:57082052..57084048-chr12:57915298..57917787,2	K562	blood:
16	chr12:57850154..57858218-chr12:57910899..57919538,20	K562	blood:
17	chr12:57848374..57850176-chr12:57916596..57918121,2	MCF-7	breast:
18	chr12:57915543..57917497-chr12:58086337..58088295,2	K562	blood:
19	chr12:57916381..57918711-chr12:58131475..58134282,2	MCF-7	breast:
20	chr12:57912759..57917021-chr12:58137187..58141030,5	MCF-7	breast:
21	chr12:57480746..57483234-chr12:57915069..57916762,2	MCF-7	breast:
22	chr12:57914860..57917603-chr12:58144909..58148802,3	K562	blood:
23	chr12:57916425..57917289-chr19:34286550..34287279,2	Hela-S3	cervix:
24	chr12:57911699..57918406-chr12:58000825..58010019,18	K562	blood:
25	chr12:57889487..57901620-chr12:57907600..57919310,30	K562	blood:
26	chr12:57912818..57918945-chr12:58145879..58149998,6	MCF-7	breast:
27	chr12:57633994..57636075-chr12:57915508..57917447,2	MCF-7	breast:
28	chr12:57912826..57917389-chr12:58135038..58139778,7	K562	blood:
29	chr12:57879869..57888452-chr12:57905809..57918310,36	K562	blood:
30	chr12:57881044..57886958-chr12:57910925..57918058,16	MCF-7	breast:
31	chr12:57022647..57024200-chr12:57914348..57917342,2	MCF-7	breast:
32	chr12:57915577..57917168-chr12:58328157..58330221,2	K562	blood:
33	chr12:57916409..57919050-chr12:57983099..57985919,3	MCF-7	breast:
34	chr12:57915614..57917377-chr12:58148904..58151083,2	K562	blood:

Variant related genes	Relation type
MIR616	TF binding region
MBD6	TF binding region
DDIT3	TF binding region
DDIT3	CpG island
MBD6	CpG island
MIR616	CpG island
ENSG00000135452	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000139269	Chromatin interaction
ENSG00000185633	Chromatin interaction
ENSG00000135446	Chromatin interaction
ENSG00000153885	Chromatin interaction
ENSG00000135454	Chromatin interaction
ENSG00000135439	Chromatin interaction
ENSG00000139266	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000110958	Chromatin interaction
ENSG00000166881	Chromatin interaction
ENSG00000255737	Chromatin interaction
ENSG00000166886	Chromatin interaction
ENSG00000179912	Chromatin interaction
ENSG00000123329	Chromatin interaction
ENSG00000257499	Chromatin interaction
ENSG00000166986	Chromatin interaction
ENSG00000076108	Chromatin interaction
ENSG00000196531	Chromatin interaction
ENSG00000258001	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000257698	Chromatin interaction
ENSG00000111087	Chromatin interaction
ENSG00000178498	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899117	chr12:57811414-57926472	Enhancers Active TSS Flanking Active TSS Weak transcription 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 miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
2	nsv899118	chr12:57811414-57946477	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
3	esv1812398	chr12:57829733-58001868	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758310	chr12:57829733-58001868	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759901	chr12:57829733-58001868	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv428283	chr12:57829733-58001868	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv469411	chr12:57844049-57921188	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv559032	chr12:57844049-57921188	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
9	nsv559033	chr12:57848639-57946477	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv899119	chr12:57851182-57923451	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers 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 miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv559034	chr12:57859932-58012233	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
14	nsv899120	chr12:57886609-57921188	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
15	esv3429239	chr12:57915210-57918058	Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	41 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57912000-57917600	Active TSS	Psoas Muscle	Psoas
2	chr12:57912400-57918600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr12:57913800-57917400	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr12:57915400-57917400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr12:57915800-57917200	Active TSS	Placenta Amnion	Placenta Amnion
6	chr12:57915800-57917200	Active TSS	Thymus	Thymus
7	chr12:57916000-57917200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr12:57916000-57917200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:57916000-57917200	Active TSS	Brain Substantia Nigra	brain
10	chr12:57916000-57917200	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr12:57916000-57917200	Active TSS	Small Intestine	intestine
12	chr12:57916000-57917400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:57916000-57917400	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr12:57916000-57917400	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr12:57916000-57917400	Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr12:57916000-57917400	Active TSS	Esophagus	oesophagus
17	chr12:57916000-57917600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:57916000-57917600	Active TSS	Gastric	stomach
19	chr12:57916000-57917600	Active TSS	Ovary	ovary
20	chr12:57916000-57917800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:57916000-57917800	Active TSS	Aorta	Aorta
22	chr12:57916200-57917000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:57916200-57917000	Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr12:57916200-57917000	Enhancers	Primary B cells from cord blood	blood
25	chr12:57916200-57917000	Active TSS	Primary T cells from cord blood	blood
26	chr12:57916200-57917000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr12:57916200-57917000	Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr12:57916200-57917000	Active TSS	Adipose Nuclei	Adipose
29	chr12:57916200-57917000	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr12:57916200-57917000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:57916200-57917000	Active TSS	Duodenum Mucosa	Duodenum
32	chr12:57916200-57917000	Active TSS	Rectal Mucosa Donor 31	rectum
33	chr12:57916200-57917000	Active TSS	Right Ventricle	heart
34	chr12:57916200-57917000	Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr12:57916200-57917200	Active TSS	H1 Cell Line	embryonic stem cell
36	chr12:57916200-57917200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:57916200-57917200	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr12:57916200-57917200	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr12:57916200-57917200	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr12:57916200-57917200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:57916200-57917200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr12:57916200-57917200	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr12:57916200-57917200	Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr12:57916200-57917200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:57916200-57917200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:57916200-57917200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:57916200-57917200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:57916200-57917200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:57916200-57917200	Active TSS	Liver	Liver
50	chr12:57916200-57917200	Active TSS	Brain Angular Gyrus	brain

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