Variant report

Variant	rs147321959
Chromosome Location	chr1:146713990-146713991
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	EBF1	chr1:146713862-146714412	GM12878	blood:	n/a	n/a
2	MAX	chr1:146713833-146715298	ECC-1	luminal epithelium:	n/a	n/a
3	POLR2A	chr1:146713962-146715070	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr1:146713941-146715310	GM19099	blood:	n/a	n/a
5	ZNF263	chr1:146713889-146715395	HEK293-T-REx	kidney:	n/a	n/a
6	POLR2A	chr1:146713919-146715429	Hela-S3	cervix:	n/a	n/a
7	STAT3	chr1:146713969-146714366	MCF10A-Er-Src	breast:	n/a	n/a
8	SMARCB1	chr1:146713969-146715384	Hela-S3	cervix:	n/a	n/a
9	TCF7L2	chr1:146713840-146715726	Hela-S3	cervix:	n/a	chr1:146713924-146713938
10	EP300	chr1:146713938-146715195	GM12878	blood:	n/a	chr1:146714608-146714624 chr1:146714539-146714555
11	SMC3	chr1:146713895-146715313	Hela-S3	cervix:	n/a	chr1:146714765-146714779 chr1:146714231-146714245 chr1:146714765-146714775
12	BRCA1	chr1:146713954-146715451	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr1:146713928-146715209	PFSK-1	brain:	n/a	n/a
14	POLR2A	chr1:146713890-146715158	K562	blood:	n/a	n/a
15	RAD21	chr1:146713811-146715151	HCT-116	colon:	n/a	chr1:146714732-146714745 chr1:146714765-146714779 chr1:146714774-146714787 chr1:146714761-146714780 chr1:146714763-146714775
16	POLR2A	chr1:146713819-146715333	GM12892	blood:	n/a	n/a
17	RCOR1	chr1:146713788-146715768	Hela-S3	cervix:	n/a	n/a
18	BACH1	chr1:146713791-146714916	H1-hESC	embryonic stem cell:	n/a	n/a
19	SP1	chr1:146713963-146714423	GM12878	blood:	n/a	chr1:146714279-146714288
20	POLR2A	chr1:146713959-146715231	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr1:146713936-146714869	ECC-1	luminal epithelium:	n/a	n/a
22	EP300	chr1:146713918-146715370	GM12878	blood:	n/a	chr1:146714608-146714624 chr1:146715308-146715318 chr1:146714539-146714555
23	GATA1	chr1:146713626-146714801	PBDE	blood:	n/a	n/a
24	POLR2A	chr1:146713971-146714946	MCF-7	breast:	n/a	n/a
25	ETS1	chr1:146713965-146714982	K562	blood:	n/a	n/a
26	KAP1	chr1:146713817-146715899	HEK293	kidney:	n/a	n/a
27	SIN3AK20	chr1:146713971-146714444	SK-N-SH	brain:	n/a	n/a
28	HEY1	chr1:146713887-146714948	HepG2	liver:	n/a	chr1:146714541-146714556 chr1:146714552-146714567
29	CTCF	chr1:146713906-146715088	HCT-116	colon:	n/a	chr1:146714231-146714244 chr1:146714770-146714778 chr1:146714765-146714778 chr1:146714231-146714244 chr1:146714763-146714781 chr1:146714758-146714779 chr1:146714764-146714780 chr1:146714230-146714246 chr1:146714229-146714247
30	MAFF	chr1:146713579-146714169	K562	blood:	n/a	n/a
31	ELK4	chr1:146713985-146714318	Hela-S3	cervix:	n/a	n/a
32	MAX	chr1:146713953-146714909	HepG2	liver:	n/a	n/a
33	CTCF	chr1:146713947-146714496	K562	blood:	n/a	chr1:146714231-146714244 chr1:146714231-146714244 chr1:146714230-146714246 chr1:146714229-146714247
34	POLR2A	chr1:146713924-146715165	K562	blood:	n/a	n/a
35	POLR2A	chr1:146713936-146715001	GM18951	blood:	n/a	n/a
36	POLR2A	chr1:146713956-146714954	K562	blood:	n/a	n/a
37	KAP1	chr1:146713914-146715178	U2OS	brain:	n/a	n/a
38	RAD21	chr1:146713871-146715029	ECC-1	luminal epithelium:	n/a	chr1:146714732-146714745 chr1:146714765-146714779 chr1:146714774-146714787 chr1:146714761-146714780 chr1:146714763-146714775
39	MAX	chr1:146713876-146715310	K562	blood:	n/a	n/a
40	MYC	chr1:146713827-146715310	K562	blood:	n/a	n/a
41	HCFC1	chr1:146713350-146715947	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:146713972-146714416	Hela-S3	cervix:	n/a	n/a
43	SMARCC2	chr1:146713775-146715351	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:146713814-146715035	U87	brain:	n/a	n/a
45	RAD21	chr1:146713990-146714956	H1-hESC	embryonic stem cell:	n/a	chr1:146714732-146714745 chr1:146714765-146714779 chr1:146714774-146714787 chr1:146714761-146714780 chr1:146714763-146714775
46	NR2F2	chr1:146713921-146714614	K562	blood:	n/a	n/a
47	RUNX3	chr1:146713952-146714995	GM12878	blood:	n/a	n/a
48	HEY1	chr1:146713930-146714982	K562	blood:	n/a	chr1:146714541-146714556 chr1:146714552-146714567
49	POLR2A	chr1:146713831-146715423	PBDE	blood:	n/a	n/a
50	CTCF	chr1:146713528-146715647	SK-N-SH	brain:	n/a	chr1:146714231-146714244 chr1:146714770-146714778 chr1:146714765-146714778 chr1:146714231-146714244 chr1:146714763-146714781 chr1:146714758-146714779 chr1:146714764-146714780 chr1:146714230-146714246 chr1:146713904-146713911 chr1:146714229-146714247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146713959-146714009	AG10803	skin:	n/a
2	chr1:146713959-146714009	PFSK-1	brain:	n/a
3	chr1:146713959-146714009	HRPEpiC	eye:	n/a
4	chr1:146713959-146714009	H1-hESC	embryonic stem cell:	embryo
5	chr1:146713959-146714009	NB4	blood:	n/a
6	chr1:146713959-146714009	Hela-S3	cervix:	n/a
7	chr1:146713959-146714009	SK-N-SH_RA	brain:	n/a
8	chr1:146713959-146714009	HMEC	breast:	n/a
9	chr1:146713959-146714009	AG04449	skin:	fetal
10	chr1:146713959-146714009	HepG2	liver:	n/a
11	chr1:146713959-146714009	A549	lung:	n/a
12	chr1:146713959-146714009	Jurkat	blood:	n/a
13	chr1:146713959-146714009	BE2_C	brain:	n/a
14	chr1:146713959-146714009	HCF	heart:	n/a
15	chr1:146713959-146714009	GM12891	blood:	n/a
16	chr1:146713959-146714009	HCM	heart:	n/a
17	chr1:146713959-146714009	Caco-2	colon:	n/a
18	chr1:146713959-146714009	NT2-D1	testis:	n/a
19	chr1:146713959-146714009	SKMC	muscle:	n/a
20	chr1:146713959-146714009	GM12878	blood:	n/a
21	chr1:146713959-146714009	HEK293	kidney:	embryo
22	chr1:146713959-146714009	RPTEC	kidney:	n/a
23	chr1:146713959-146714009	NH-A	brain:	n/a
24	chr1:146713959-146714009	ovcar-3	ovarian:	n/a
25	chr1:146713959-146714009	SK-N-MC	brain:	n/a
26	chr1:146713959-146714009	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:146713959-146714009	HUVEC	blood vessel:	n/a
28	chr1:146713959-146714009	NHDF-neo	bronchial:	n/a
29	chr1:146713959-146714009	BJ	skin:	n/a
30	chr1:146713959-146714009	HNPCEpiC	eye:	n/a
31	chr1:146713959-146714009	AG09319	gingival:	n/a
32	chr1:146713959-146714009	ProgFib	skin:	n/a
33	chr1:146713959-146714009	U87	brain:	n/a
34	chr1:146713959-146714009	AG09309	skin:	n/a
35	chr1:146713959-146714009	GM12892	blood:	n/a
36	chr1:146713959-146714009	PANC-1	pancreas:	n/a
37	chr1:146713959-146714009	IMR90	lung:	fetal
38	chr1:146713959-146714009	GM06990	blood:	n/a
39	chr1:146713959-146714009	GM19239	blood:	n/a
40	chr1:146713959-146714009	PrEC	prostate:	n/a
41	chr1:146713959-146714009	HIPEpiC	eye:	n/a
42	chr1:146713959-146714009	HL-60	blood:	n/a
43	chr1:146713959-146714009	SAEC	small airway:	n/a
44	chr1:146713959-146714009	CMK	blood:	n/a
45	chr1:146713959-146714009	ECC-1	luminal epithelium:	n/a
46	chr1:146713959-146714009	MCF10A-Er-Src	breast:	n/a
47	chr1:146713959-146714009	AoSMC	blood vessel:	n/a
48	chr1:146713959-146714009	T-47D	breast:	n/a
49	chr1:146713959-146714009	Hepatocyte	liver:	n/a
50	chr1:146713959-146714009	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:146637222..146651713-chr1:146712141..146718911,44	MCF-7	breast:
2	chr1:146712756..146714985-chr9:19378272..19380601,2	MCF-7	breast:
3	chr1:146632272..146634531-chr1:146713179..146715784,3	MCF-7	breast:
4	chr1:146649315..146651856-chr1:146712649..146716301,4	MCF-7	breast:
5	chr1:146713799..146714746-chr7:86781364..86782270,2	Hela-S3	cervix:
6	chr1:146629607..146632064-chr1:146712714..146714253,2	MCF-7	breast:
7	chr1:146554717..146557790-chr1:146713275..146715735,7	MCF-7	breast:
8	chr1:146550590..146559110-chr1:146711930..146718078,31	K562	blood:
9	chr1:146638562..146647588-chr1:146711453..146720391,22	K562	blood:
10	chr1:146552515..146557737-chr1:146711619..146718083,31	K562	blood:
11	chr1:146640645..146647502-chr1:146711418..146719354,29	K562	blood:
12	chr1:146643464..146645140-chr1:146713602..146715704,127	MCF-7	breast:
13	chr1:146643751..146644645-chr1:146713680..146714742,5	MCF-7	breast:
14	chr1:146642817..146644911-chr1:146712966..146715242,14	K562	blood:
15	chr1:146554504..146557399-chr1:146713775..146716499,4	MCF-7	breast:
16	chr1:28975066..28975586-chr1:146713775..146714464,2	NB4	blood:
17	chr1:146643597..146644883-chr1:146713838..146714581,3	MCF-7	breast:
18	chr1:146713889..146714482-chr1:207494791..207495360,2	Hela-S3	cervix:
19	chr1:146696837..146698411-chr1:146712690..146714325,2	K562	blood:
20	chr1:146643493..146644893-chr1:146713471..146715076,53	MCF-7	breast:
21	chr1:146638044..146647556-chr1:146707628..146717159,48	MCF-7	breast:

Variant related genes	Relation type
CHD1L	TF binding region
CHD1L	CpG island
ENSG00000135164	Chromatin interaction
ENSG00000230832	Chromatin interaction
ENSG00000196352	Chromatin interaction
ENSG00000273071	Chromatin interaction
ENSG00000224046	Chromatin interaction
ENSG00000237188	Chromatin interaction
ENSG00000180867	Chromatin interaction
ENSG00000201142	Chromatin interaction
ENSG00000137154	Chromatin interaction
ENSG00000271721	Chromatin interaction
ENSG00000131791	Chromatin interaction
ENSG00000131781	Chromatin interaction
ENSG00000270103	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872251	chr1:146152553-146803630	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS 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 miRNA target site	95 gene(s)	inside rSNPs	diseases
2	nsv872252	chr1:146471863-147398135	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
3	nsv999546	chr1:146507577-147356574	Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
4	nsv535123	chr1:146507577-147356574	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer 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	110 gene(s)	inside rSNPs	diseases
5	nsv492188	chr1:146507649-147381479	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
6	nsv916754	chr1:146507711-147417736	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
7	nsv547673	chr1:146510112-147398135	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
8	nsv547674	chr1:146522722-147396797	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv998341	chr1:146531446-147384720	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
10	nsv535124	chr1:146531446-147384720	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
11	nsv1003493	chr1:146531446-147389944	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
12	nsv998209	chr1:146543722-147384720	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription 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	110 gene(s)	inside rSNPs	diseases
13	nsv535126	chr1:146543722-147384720	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
14	nsv872255	chr1:146550780-146969712	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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	93 gene(s)	inside rSNPs	diseases
15	nsv872256	chr1:146556596-147410973	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1012331	chr1:146603479-147384720	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
17	nsv535131	chr1:146603479-147384720	Genic enhancers Strong transcription Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
18	nsv1009943	chr1:146618929-146893851	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
19	nsv535132	chr1:146618929-146893851	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
20	nsv872257	chr1:146643555-146724923	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
21	nsv437047	chr1:146643555-146841602	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
22	nsv1005809	chr1:146647822-146886419	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
23	nsv535134	chr1:146647822-146886419	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv1004849	chr1:146661516-147286826	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
25	nsv535135	chr1:146661516-147286826	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS 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
26	nsv547676	chr1:146686228-146996047	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
27	nsv872259	chr1:146688941-146724923	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
28	esv3325681	chr1:146713353-146715901	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146709200-146714200	Weak transcription	Gastric	stomach
2	chr1:146709400-146714000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:146709400-146714000	Weak transcription	Esophagus	oesophagus
4	chr1:146709400-146714200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:146712600-146714000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:146712600-146714000	Weak transcription	Pancreas	Pancrea
7	chr1:146712600-146714200	Weak transcription	Lung	lung
8	chr1:146713200-146714200	Flanking Active TSS	Liver	Liver
9	chr1:146713400-146714000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr1:146713400-146714200	Flanking Active TSS	Dnd41	blood
11	chr1:146713400-146714200	Flanking Active TSS	HepG2	liver
12	chr1:146713600-146714000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:146713600-146714000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:146713600-146714000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr1:146713600-146714000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr1:146713600-146714000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:146713600-146714000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr1:146713600-146714000	Flanking Active TSS	Brain Angular Gyrus	brain
19	chr1:146713600-146714000	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr1:146713600-146714000	Flanking Active TSS	A549	lung
21	chr1:146713600-146714200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:146713600-146714200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:146713600-146714200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:146713600-146714200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr1:146713600-146714200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr1:146713600-146714200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr1:146713600-146714200	Flanking Active TSS	Osteobl	bone
28	chr1:146713600-146714400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr1:146713600-146714400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:146713800-146714000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr1:146713800-146714000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr1:146713800-146714000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr1:146713800-146714000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:146713800-146714000	Enhancers	Primary B cells from cord blood	blood
35	chr1:146713800-146714000	Enhancers	Primary T cells from cord blood	blood
36	chr1:146713800-146714000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:146713800-146714000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:146713800-146714000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:146713800-146714000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:146713800-146714000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:146713800-146714000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:146713800-146714000	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr1:146713800-146714000	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr1:146713800-146714000	Flanking Active TSS	Fetal Heart	heart
45	chr1:146713800-146714000	Enhancers	Fetal Muscle Leg	muscle
46	chr1:146713800-146714000	Enhancers	Placenta	Placenta
47	chr1:146713800-146714000	Enhancers	Fetal Stomach	stomach
48	chr1:146713800-146714000	Active TSS	Right Atrium	heart
49	chr1:146713800-146714000	Enhancers	Thymus	Thymus
50	chr1:146713800-146714000	Flanking Active TSS	NHDF-Ad	bronchial

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