Variant report

Variant	rs6695183
Chromosome Location	chr1:113616577-113616578
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	CBX3	chr1:113614710-113616713	K562	blood:	n/a	n/a
2	POLR2A	chr1:113616523-113616656	MCF-7	breast:	n/a	n/a
3	RCOR1	chr1:113614768-113616833	K562	blood:	n/a	n/a
4	POLR2A	chr1:113615181-113616737	K562	blood:	n/a	n/a
5	POLR2A	chr1:113614912-113616753	K562	blood:	n/a	n/a
6	CTCF	chr1:113614616-113616959	SK-N-SH	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
7	TAL1	chr1:113614718-113616753	K562	blood:	n/a	n/a
8	MXI1	chr1:113615210-113616768	Hela-S3	cervix:	n/a	n/a
9	YY1	chr1:113615226-113616631	SK-N-SH	brain:	n/a	n/a
10	CTCF	chr1:113614771-113616621	HCT-116	colon:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
11	MAZ	chr1:113615043-113616927	IMR90	lung:	n/a	chr1:113616695-113616703 chr1:113616690-113616703
12	MYC	chr1:113614710-113616768	K562	blood:	n/a	chr1:113614819-113614829 chr1:113616695-113616703 chr1:113616690-113616703
13	CHD1	chr1:113616515-113616608	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAZ	chr1:113615211-113616807	GM12878	blood:	n/a	chr1:113616695-113616703 chr1:113616690-113616703
15	POLR2A	chr1:113615544-113616586	ECC-1	luminal epithelium:	n/a	n/a
16	SMARCC1	chr1:113614967-113616684	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr1:113615202-113617133	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:113614798-113616918	K562	blood:	n/a	n/a
19	IRF1	chr1:113614788-113616710	K562	blood:	n/a	chr1:113615772-113615781
20	SMC3	chr1:113614999-113616652	Hela-S3	cervix:	n/a	chr1:113615389-113615399 chr1:113615385-113615399
21	RAD21	chr1:113614821-113616959	SK-N-SH	brain:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
22	BHLHE40	chr1:113615144-113616850	GM12878	blood:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700
23	USF1	chr1:113616409-113616818	K562	blood:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700
24	MAX	chr1:113615221-113616824	NB4	blood:	n/a	chr1:113616695-113616703 chr1:113616690-113616703
25	CHD1	chr1:113615205-113616715	GM12878	blood:	n/a	n/a
26	MAZ	chr1:113615211-113616645	Hela-S3	cervix:	n/a	n/a
27	BHLHE40	chr1:113614776-113616877	K562	blood:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700
28	STAT5A	chr1:113615346-113616596	GM12878	blood:	n/a	n/a
29	JUN	chr1:113614768-113616782	K562	blood:	n/a	n/a
30	USF1	chr1:113616521-113616846	K562	blood:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700
31	CTCF	chr1:113614711-113616719	A549	lung:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
32	MYC	chr1:113614773-113616870	K562	blood:	n/a	chr1:113614819-113614829 chr1:113616695-113616703 chr1:113616690-113616703
33	TEAD4	chr1:113614605-113616826	K562	blood:	n/a	n/a
34	SIN3AK20	chr1:113615224-113616720	K562	blood:	n/a	n/a
35	USF1	chr1:113616473-113616808	SK-N-SH_RA	brain:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700
36	JUN	chr1:113614096-113617273	K562	blood:	n/a	chr1:113617087-113617097 chr1:113617087-113617097 chr1:113617087-113617097 chr1:113617087-113617097
37	POLR2A	chr1:113615213-113617173	GM12891	blood:	n/a	n/a
38	POLR2A	chr1:113616516-113616668	MCF10A-Er-Src	breast:	n/a	n/a
39	CTCF	chr1:113616520-113616670	HBMEC	blood vessel:	n/a	n/a
40	YY1	chr1:113615142-113616728	GM12878	blood:	n/a	n/a
41	RCOR1	chr1:113614682-113616779	K562	blood:	n/a	n/a
42	USF2	chr1:113616281-113616860	Hela-S3	cervix:	n/a	chr1:113616692-113616701 chr1:113616691-113616702 chr1:113616692-113616701 chr1:113616691-113616700
43	UBTF	chr1:113614847-113616611	K562	blood:	n/a	n/a
44	HCFC1	chr1:113614825-113617080	Hela-S3	cervix:	n/a	n/a
45	MAX	chr1:113615127-113616827	K562	blood:	n/a	chr1:113616695-113616703 chr1:113616690-113616703
46	NR2F2	chr1:113614565-113616714	K562	blood:	n/a	n/a
47	REST	chr1:113614718-113616649	H1-neurons	neurons:	n/a	n/a
48	SIN3A	chr1:113615200-113616736	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:113615202-113616674	K562	blood:	n/a	n/a
50	USF1	chr1:113616529-113616895	H1-hESC	embryonic stem cell:	n/a	chr1:113616692-113616701 chr1:113616692-113616701 chr1:113616691-113616700

No.	Distal block	Cell Line	Cell type
1	chr1:113614064..113616964-chr1:113668302..113669880,2	K562	blood:
2	chr1:113442578..113444928-chr1:113615994..113617542,2	K562	blood:
3	chr1:113615753..113616585-chr11:62608645..62609638,3	Hela-S3	cervix:
4	chr1:113616013..113618025-chr1:113688637..113691001,2	MCF-7	breast:
5	chr1:113493791..113500715-chr1:113613796..113618010,15	K562	blood:
6	chr1:113615667..113617631-chr6:26055280..26057308,2	MCF-7	breast:
7	chr1:113615839..113617741-chr1:113618615..113621229,2	K562	blood:
8	chr1:113257532..113261488-chr1:113614794..113617265,4	K562	blood:
9	chr1:113615878..113618493-chr1:113649795..113652119,3	MCF-7	breast:
10	chr1:113495059..113500488-chr1:113613593..113618010,11	K562	blood:
11	chr1:113258208..113260404-chr1:113615515..113617358,3	MCF-7	breast:
12	chr1:113615969..113617756-chr1:113641102..113642672,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238198	TF binding region
ENSG00000198799	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000155367	Chromatin interaction
ENSG00000155380	Chromatin interaction
ENSG00000226419	Chromatin interaction
ENSG00000261595	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000237278	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs11102584	0.90[ASN][1000 genomes]
rs11102586	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11102588	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11102592	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs12031658	1.00[CHB][hapmap]
rs12071491	0.86[EUR][1000 genomes]
rs12117273	1.00[EUR][1000 genomes]
rs12118061	0.83[EUR][1000 genomes]
rs12118532	1.00[EUR][1000 genomes]
rs12119387	0.83[EUR][1000 genomes]
rs12120401	0.83[EUR][1000 genomes]
rs12120441	0.83[EUR][1000 genomes]
rs12120738	1.00[EUR][1000 genomes]
rs12123072	1.00[EUR][1000 genomes]
rs12123519	1.00[EUR][1000 genomes]
rs12123601	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12125675	0.83[EUR][1000 genomes]
rs12125708	0.83[EUR][1000 genomes]
rs12126304	0.83[EUR][1000 genomes]
rs12127415	0.83[EUR][1000 genomes]
rs12128658	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12129858	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12133057	1.00[EUR][1000 genomes]
rs12136395	0.83[EUR][1000 genomes]
rs12136941	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12137299	1.00[EUR][1000 genomes]
rs12139726	0.83[EUR][1000 genomes]
rs12139899	0.83[EUR][1000 genomes]
rs12140067	0.86[EUR][1000 genomes]
rs12140810	0.83[EUR][1000 genomes]
rs12141415	1.00[EUR][1000 genomes]
rs12141540	0.83[EUR][1000 genomes]
rs12141541	0.83[EUR][1000 genomes]
rs12142449	0.83[EUR][1000 genomes]
rs12142475	0.83[EUR][1000 genomes]
rs12142510	0.83[EUR][1000 genomes]
rs12143171	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12143341	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12143430	0.83[EUR][1000 genomes]
rs12145713	0.83[EUR][1000 genomes]
rs12145738	0.83[EUR][1000 genomes]
rs1216767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216769	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216793	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216798	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216802	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216805	0.90[ASN][1000 genomes]
rs1216807	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216808	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216810	0.90[ASN][1000 genomes]
rs1216812	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216813	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12184272	1.00[EUR][1000 genomes]
rs12184320	1.00[EUR][1000 genomes]
rs12744661	1.00[EUR][1000 genomes]
rs1310142	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1618794	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17030871	0.89[ASN][1000 genomes]
rs17031006	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1728227	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1728229	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1728240	0.86[EUR][1000 genomes]
rs1766864	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1766865	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1778016	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1778017	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1778019	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41296184	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4839291	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4839292	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6670587	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6688685	0.82[YRI][hapmap]
rs74111210	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74111213	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7518115	0.83[EUR][1000 genomes]
rs7531847	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7538813	0.86[EUR][1000 genomes]
rs7541246	0.83[EUR][1000 genomes]
rs7541520	0.83[EUR][1000 genomes]
rs7541703	0.83[EUR][1000 genomes]
rs7545814	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs946215	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS 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	100 gene(s)	inside rSNPs	diseases
7	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers 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 target site	68 gene(s)	inside rSNPs	diseases
8	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	69 gene(s)	inside rSNPs	diseases
9	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv946146	chr1:113567302-113640814	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv508537	chr1:113590343-113635803	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv437002	chr1:113592588-113658887	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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	13 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	chr1:113614800-113616600	Active TSS	Brain Hippocampus Middle	brain
2	chr1:113614800-113617000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr1:113614800-113617200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:113615000-113616600	Active TSS	Fetal Kidney	kidney
5	chr1:113615000-113616600	Active TSS	Thymus	Thymus
6	chr1:113615000-113616800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:113615000-113617000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:113615000-113617200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:113615000-113617200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:113615000-113617200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:113615000-113617200	Active TSS	Fetal Muscle Trunk	muscle
12	chr1:113615000-113617200	Active TSS	HSMMtube	muscle
13	chr1:113615000-113617200	Active TSS	NHDF-Ad	bronchial
14	chr1:113615000-113617400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:113615000-113617400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:113615000-113617400	Active TSS	Colonic Mucosa	Colon
17	chr1:113615000-113617400	Active TSS	NHLF	lung
18	chr1:113615000-113617800	Active TSS	Right Ventricle	heart
19	chr1:113615200-113616600	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr1:113615200-113616600	Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr1:113615200-113616600	Active TSS	Fetal Brain Female	brain
22	chr1:113615200-113616600	Active TSS	Pancreas	Pancrea
23	chr1:113615200-113616600	Active TSS	HUVEC	blood vessel
24	chr1:113615200-113616800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:113615200-113616800	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr1:113615200-113616800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:113615200-113616800	Active TSS	Muscle Satellite Cultured Cells	--
28	chr1:113615200-113616800	Active TSS	Esophagus	oesophagus
29	chr1:113615200-113616800	Active TSS	Placenta	Placenta
30	chr1:113615200-113616800	Active TSS	Gastric	stomach
31	chr1:113615200-113616800	Active TSS	Lung	lung
32	chr1:113615200-113617000	Active TSS	H1 Cell Line	embryonic stem cell
33	chr1:113615200-113617000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:113615200-113617000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:113615200-113617000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:113615200-113617000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr1:113615200-113617000	Active TSS	Aorta	Aorta
38	chr1:113615200-113617000	Active TSS	Fetal Heart	heart
39	chr1:113615200-113617000	Active TSS	Ovary	ovary
40	chr1:113615200-113617000	Active TSS	Psoas Muscle	Psoas
41	chr1:113615200-113617000	Active TSS	Small Intestine	intestine
42	chr1:113615200-113617000	Active TSS	GM12878-XiMat	blood
43	chr1:113615200-113617200	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr1:113615200-113617200	Active TSS	H9 Cell Line	embryonic stem cell
45	chr1:113615200-113617200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:113615200-113617200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:113615200-113617200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr1:113615200-113617200	Active TSS	Left Ventricle	heart
49	chr1:113615200-113617400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:113615200-113617400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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