Variant report

Variant	rs782584
Chromosome Location	chr2:55921116-55921117
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr2:55920955-55921181	MCF10A-Er-Src	breast:	n/a	chr2:55920991-55921000
2	TAF1	chr2:55920716-55921144	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr2:55920758-55921128	ECC-1	luminal epithelium:	n/a	n/a
4	EP300	chr2:55920688-55921287	GM12878	blood:	n/a	n/a
5	POLR2A	chr2:55920691-55921261	HCT-116	colon:	n/a	n/a
6	MXI1	chr2:55920744-55921186	H1-hESC	embryonic stem cell:	n/a	n/a
7	E2F4	chr2:55920912-55921249	MCF10A-Er-Src	breast:	n/a	chr2:55920993-55921002
8	REST	chr2:55920678-55921154	PFSK-1	brain:	n/a	chr2:55921008-55921021
9	MYC	chr2:55920660-55921233	MCF-7	breast:	n/a	chr2:55920968-55920975
10	REST	chr2:55920634-55921235	A549	lung:	n/a	chr2:55921008-55921021
11	TAL1	chr2:55920746-55921226	K562	blood:	n/a	n/a
12	CEBPD	chr2:55920734-55921134	HepG2	liver:	n/a	n/a
13	POLR2A	chr2:55920580-55921234	A549	lung:	n/a	n/a
14	TAF1	chr2:55920631-55921174	H1-hESC	embryonic stem cell:	n/a	n/a
15	EP300	chr2:55920789-55921402	HepG2	liver:	n/a	n/a
16	POLR2A	chr2:55920753-55921278	U87	brain:	n/a	n/a
17	SIN3AK20	chr2:55920682-55921215	H1-hESC	embryonic stem cell:	n/a	n/a
18	RELA	chr2:55920598-55921229	GM15510	blood:	n/a	n/a
19	ELF1	chr2:55920788-55921322	A549	lung:	n/a	n/a
20	MYC	chr2:55920563-55921236	MCF10A-Er-Src	breast:	n/a	chr2:55920968-55920975
21	E2F6	chr2:55920470-55921363	H1-hESC	embryonic stem cell:	n/a	chr2:55920993-55921002
22	NFATC1	chr2:55920703-55921291	GM12878	blood:	n/a	n/a
23	ARID3A	chr2:55920973-55921350	K562	blood:	n/a	n/a
24	CREB1	chr2:55920634-55921202	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:55920783-55921309	A549	lung:	n/a	chr2:55920993-55921001
26	POLR2A	chr2:55920668-55921321	H1-neurons	neurons:	n/a	n/a
27	FOS	chr2:55920957-55921124	MCF10A-Er-Src	breast:	n/a	chr2:55920991-55921000
28	CEBPB	chr2:55920861-55921278	A549	lung:	n/a	chr2:55920993-55921001
29	USF1	chr2:55920751-55921227	A549	lung:	n/a	n/a
30	ELF1	chr2:55920638-55921366	A549	lung:	n/a	chr2:55920646-55920657
31	TEAD4	chr2:55920730-55921185	H1-hESC	embryonic stem cell:	n/a	n/a
32	TCF12	chr2:55920580-55921332	ECC-1	luminal epithelium:	n/a	n/a
33	USF1	chr2:55920580-55921230	ECC-1	luminal epithelium:	n/a	n/a
34	MAZ	chr2:55920721-55921242	K562	blood:	n/a	chr2:55920968-55920975
35	MAX	chr2:55920765-55921189	K562	blood:	n/a	chr2:55920968-55920975
36	TAF1	chr2:55920197-55921194	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr2:55920671-55921208	HepG2	liver:	n/a	n/a
38	FOS	chr2:55920932-55921157	MCF10A-Er-Src	breast:	n/a	chr2:55920991-55921000
39	POLR2A	chr2:55920456-55921302	PFSK-1	brain:	n/a	n/a
40	BHLHE40	chr2:55920674-55921168	HepG2	liver:	n/a	n/a
41	GABPA	chr2:55920775-55921124	K562	blood:	n/a	n/a
42	FOXM1	chr2:55920665-55921304	GM12878	blood:	n/a	n/a
43	SIN3AK20	chr2:55920711-55921262	A549	lung:	n/a	n/a
44	SIN3AK20	chr2:55920652-55921171	HepG2	liver:	n/a	n/a
45	MAX	chr2:55920373-55921450	A549	lung:	n/a	chr2:55920968-55920975
46	TAF1	chr2:55920672-55921158	HepG2	liver:	n/a	n/a
47	ELF1	chr2:55920796-55921232	HepG2	liver:	n/a	n/a
48	HDAC2	chr2:55920723-55921319	HepG2	liver:	n/a	chr2:55921266-55921275
49	TAF1	chr2:55920693-55921133	GM12891	blood:	n/a	n/a
50	REST	chr2:55920470-55921399	A549	lung:	n/a	chr2:55921008-55921021

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55921072-55921122	T-47D	breast:	n/a
2	chr2:55921072-55921122	HEEpiC	esophagus:	n/a
3	chr2:55921094-55921144	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:55921072-55921122	HRPEpiC	eye:	n/a
5	chr2:55921094-55921144	BE2_C	brain:	n/a
6	chr2:55921094-55921144	H1-hESC	embryonic stem cell:	embryo
7	chr2:55921072-55921122	AG04449	skin:	fetal
8	chr2:55921072-55921122	GM12891	blood:	n/a
9	chr2:55921094-55921144	HCF	heart:	n/a
10	chr2:55921094-55921144	SAEC	small airway:	n/a
11	chr2:55921094-55921144	NHDF-neo	bronchial:	n/a
12	chr2:55921072-55921122	Hepatocyte	liver:	n/a
13	chr2:55921072-55921122	SAEC	small airway:	n/a
14	chr2:55921094-55921144	HRCEpiC	kidney:	n/a
15	chr2:55921072-55921122	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:55921072-55921122	MCF-7	breast:	n/a
17	chr2:55921072-55921122	HL-60	blood:	n/a
18	chr2:55921094-55921144	Hepatocyte	liver:	n/a
19	chr2:55921094-55921144	SKMC	muscle:	n/a
20	chr2:55921094-55921144	HUVEC	blood vessel:	n/a
21	chr2:55921072-55921122	MCF10A-Er-Src	breast:	n/a
22	chr2:55921072-55921122	HRCEpiC	kidney:	n/a
23	chr2:55921094-55921144	HRE	kidney:	n/a
24	chr2:55921072-55921122	PrEC	prostate:	n/a
25	chr2:55921072-55921122	LNCaP	prostate:	n/a
26	chr2:55921072-55921122	PANC-1	pancreas:	n/a
27	chr2:55921072-55921122	SK-N-SH_RA	brain:	n/a
28	chr2:55921072-55921122	BE2_C	brain:	n/a
29	chr2:55921072-55921122	HIPEpiC	eye:	n/a
30	chr2:55921094-55921144	AG10803	skin:	n/a
31	chr2:55921072-55921122	H1-hESC	embryonic stem cell:	embryo
32	chr2:55921094-55921144	ECC-1	luminal epithelium:	n/a
33	chr2:55921094-55921144	GM12878	blood:	n/a
34	chr2:55921094-55921144	SK-N-MC	brain:	n/a
35	chr2:55921094-55921144	PrEC	prostate:	n/a
36	chr2:55921094-55921144	Hela-S3	cervix:	n/a
37	chr2:55921094-55921144	HEK293	kidney:	embryo
38	chr2:55921094-55921144	AoSMC	blood vessel:	n/a
39	chr2:55921094-55921144	GM12892	blood:	n/a
40	chr2:55921072-55921122	ProgFib	skin:	n/a
41	chr2:55921094-55921144	NHBE	bronchial:	n/a
42	chr2:55921072-55921122	K562	blood:	n/a
43	chr2:55921072-55921122	PFSK-1	brain:	n/a
44	chr2:55921094-55921144	HAEpiC	amniotic membrane:	n/a
45	chr2:55921072-55921122	GM19239	blood:	n/a
46	chr2:55921094-55921144	HRPEpiC	eye:	n/a
47	chr2:55921094-55921144	HNPCEpiC	eye:	n/a
48	chr2:55921072-55921122	NB4	blood:	n/a
49	chr2:55921072-55921122	Caco-2	colon:	n/a
50	chr2:55921072-55921122	SK-N-SH	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:55920582..55922485-chr2:56215430..56218121,2	K562	blood:
2	chr2:55841795..55844862-chr2:55919047..55922552,3	K562	blood:
3	chr2:55843362..55845607-chr2:55918078..55921710,3	K562	blood:
4	chr17:62222684..62223474-chr2:55920600..55921160,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
PNPT1	TF binding region
PNPT1	CpG island
ENSG00000207798	Chromatin interaction
ENSG00000272606	Chromatin interaction
ENSG00000138041	Chromatin interaction
ENSG00000199753	Chromatin interaction
ENSG00000266402	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10207590	0.81[AFR][1000 genomes]
rs10460508	0.89[CEU][hapmap];0.94[GIH][hapmap];0.83[JPT][hapmap];0.80[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10496050	0.85[CEU][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.86[YRI][hapmap]
rs1084522	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap]
rs1084525	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.92[MEX][hapmap];0.93[MKK][hapmap];0.86[YRI][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12617719	0.80[AFR][1000 genomes]
rs17278044	0.85[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs17369191	0.85[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap]
rs1823893	0.85[CEU][hapmap];0.81[JPT][hapmap];0.88[YRI][hapmap]
rs1975484	0.85[CEU][hapmap];0.81[JPT][hapmap]
rs1975487	0.84[CEU][hapmap];0.90[JPT][hapmap]
rs2586950	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs2586954	0.89[CEU][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.90[LWK][hapmap];0.96[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2586969	0.88[YRI][hapmap]
rs2586970	0.88[YRI][hapmap]
rs2627765	0.92[MEX][hapmap];0.86[MKK][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes]
rs2627766	0.84[AMR][1000 genomes]
rs2627767	0.86[AMR][1000 genomes]
rs2627769	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2627772	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2627773	0.96[CEU][hapmap];0.83[JPT][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2627775	0.86[CHB][hapmap];0.83[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.80[MKK][hapmap];0.86[YRI][hapmap]
rs2627776	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs2627779	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35504023	0.85[CEU][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap];0.86[YRI][hapmap]
rs4290693	0.85[CEU][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.84[TSI][hapmap];0.86[YRI][hapmap]
rs4312532	0.83[YRI][hapmap]
rs62165255	0.87[AMR][1000 genomes]
rs6545506	0.85[CEU][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap];0.86[YRI][hapmap]
rs706548	1.00[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs7582278	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs7589673	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs782566	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs782567	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs782568	0.89[CEU][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.80[LWK][hapmap];0.96[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs782572	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs782573	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs782585	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs782586	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap];0.86[YRI][hapmap]
rs782588	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap]
rs782590	0.81[CEU][hapmap];0.85[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap]
rs782595	0.85[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs782599	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap]
rs782602	1.00[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.85[MKK][hapmap];0.84[TSI][hapmap];0.86[YRI][hapmap]
rs782606	0.89[CEU][hapmap];0.85[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.90[LWK][hapmap];0.96[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs782607	0.82[AMR][1000 genomes]
rs782619	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs782622	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs782629	0.96[CEU][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs782630	0.96[CEU][hapmap];0.82[JPT][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs782632	0.96[CEU][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs782633	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs782634	0.82[CEU][hapmap];0.83[JPT][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs782637	0.92[CEU][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs782641	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs782642	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs782644	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs782652	0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.85[MKK][hapmap];0.91[TSI][hapmap];0.82[YRI][hapmap]
rs809732	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs935177	0.88[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv834080	chr2:55741036-55927928	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS 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 miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2757798	chr2:55747239-55981074	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv2759050	chr2:55747239-55981074	Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1008452	chr2:55809191-55987274	Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	esv2762645	chr2:55892248-55963418	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv2760573	chr2:55903016-55941440	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv9802	chr2:55910254-55939253	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	esv16137	chr2:55910848-55938746	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv442740	chr2:55914790-55938579	Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv514069	chr2:55914952-55938116	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55918400-55921600	Active TSS	GM12878-XiMat	blood
2	chr2:55919400-55921400	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr2:55919400-55921400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:55919400-55921800	Active TSS	A549	lung
5	chr2:55919600-55921200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:55919600-55921400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:55919600-55921400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr2:55919600-55921400	Active TSS	HMEC	breast
9	chr2:55919600-55921600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:55919800-55921200	Active TSS	H1 Cell Line	embryonic stem cell
11	chr2:55919800-55921200	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr2:55919800-55921200	Active TSS	HSMM	muscle
13	chr2:55919800-55921400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:55919800-55921400	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr2:55919800-55921400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:55919800-55921400	Active TSS	Fetal Intestine Large	intestine
17	chr2:55919800-55921600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:55919800-55921600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:55919800-55921600	Active TSS	Duodenum Smooth Muscle	Duodenum
20	chr2:55919800-55921600	Active TSS	Fetal Intestine Small	intestine
21	chr2:55919800-55921600	Active TSS	Stomach Smooth Muscle	stomach
22	chr2:55919800-55922400	Active TSS	Right Atrium	heart
23	chr2:55920000-55921200	Active TSS	H9 Cell Line	embryonic stem cell
24	chr2:55920000-55921200	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr2:55920000-55921200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr2:55920000-55921200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:55920000-55921200	Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr2:55920000-55921200	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr2:55920000-55921200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:55920000-55921200	Active TSS	Esophagus	oesophagus
31	chr2:55920000-55921200	Active TSS	Hela-S3	cervix
32	chr2:55920000-55921200	Active TSS	K562	blood
33	chr2:55920000-55921200	Active TSS	NHEK	skin
34	chr2:55920000-55921400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:55920000-55921400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:55920000-55921400	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr2:55920000-55921400	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr2:55920000-55921400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:55920000-55921400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:55920000-55921400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr2:55920000-55921400	Active TSS	Brain Angular Gyrus	brain
42	chr2:55920000-55921400	Active TSS	Brain Cingulate Gyrus	brain
43	chr2:55920000-55921400	Active TSS	Colonic Mucosa	Colon
44	chr2:55920000-55921400	Active TSS	Colon Smooth Muscle	Colon
45	chr2:55920000-55921400	Active TSS	Fetal Kidney	kidney
46	chr2:55920000-55921400	Active TSS	Fetal Thymus	thymus
47	chr2:55920000-55921400	Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr2:55920000-55921400	Active TSS	HSMMtube	muscle
49	chr2:55920000-55921600	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:55920000-55921600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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