Variant report

Variant	rs2500414
Chromosome Location	chr20:25387911-25387912
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	NFYB	chr20:25387719-25388615	GM12878	blood:	n/a	chr20:25388292-25388307 chr20:25388290-25388305 chr20:25388290-25388305 chr20:25388291-25388305
2	REST	chr20:25387857-25388895	H1-neurons	neurons:	n/a	n/a
3	FOXM1	chr20:25387900-25388688	GM12878	blood:	n/a	n/a
4	NFIC	chr20:25387797-25388696	HepG2	liver:	n/a	n/a
5	MAX	chr20:25387890-25388778	HepG2	liver:	n/a	n/a
6	POLR2A	chr20:25387869-25388687	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr20:25387798-25388586	GM12878	blood:	n/a	n/a
8	FOXM1	chr20:25387875-25388793	ECC-1	luminal epithelium:	n/a	n/a
9	POLR2A	chr20:25387889-25388719	HUVEC	blood vessel:	n/a	n/a
10	HDAC2	chr20:25387906-25388619	MCF-7	breast:	n/a	n/a
11	RAD21	chr20:25387862-25388559	HepG2	liver:	n/a	n/a
12	POLR2A	chr20:25387884-25388746	HL-60	blood:	n/a	n/a
13	KAP1	chr20:25387769-25388856	HEK293	kidney:	n/a	chr20:25388681-25388689
14	TEAD4	chr20:25387862-25388713	SK-N-SH	brain:	n/a	n/a
15	POLR2A	chr20:25387770-25388806	PFSK-1	brain:	n/a	n/a
16	TCF12	chr20:25387644-25389162	A549	lung:	n/a	n/a
17	TEAD4	chr20:25387583-25388844	HepG2	liver:	n/a	n/a
18	RCOR1	chr20:25387888-25388966	K562	blood:	n/a	n/a
19	RFX5	chr20:25387779-25388674	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr20:25387720-25389178	H1-hESC	embryonic stem cell:	n/a	n/a
21	ZBTB7A	chr20:25387887-25388642	ECC-1	luminal epithelium:	n/a	n/a
22	POLR2A	chr20:25387776-25389318	HepG2	liver:	n/a	n/a
23	MAX	chr20:25387838-25388859	HCT-116	colon:	n/a	n/a
24	MAX	chr20:25387769-25388877	HepG2	liver:	n/a	n/a
25	POLR2A	chr20:25387877-25388815	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr20:25387843-25389068	HUVEC	blood vessel:	n/a	n/a
27	SP1	chr20:25387872-25388814	HCT-116	colon:	n/a	chr20:25388583-25388595 chr20:25388583-25388595 chr20:25388585-25388594 chr20:25388219-25388231 chr20:25388195-25388204 chr20:25388584-25388593 chr20:25388585-25388594 chr20:25388584-25388594 chr20:25388219-25388231 chr20:25388283-25388304 chr20:25388228-25388239 chr20:25388194-25388203 chr20:25388220-25388230 chr20:25388193-25388204 chr20:25388195-25388204 chr20:25388228-25388240 chr20:25388193-25388205
28	NFIC	chr20:25387892-25388587	HepG2	liver:	n/a	n/a
29	PML	chr20:25387783-25388816	GM12878	blood:	n/a	chr20:25388681-25388689
30	NFIC	chr20:25387777-25388717	GM12878	blood:	n/a	n/a
31	HEY1	chr20:25387868-25388666	HepG2	liver:	n/a	n/a
32	E2F4	chr20:25387607-25389100	MCF10A-Er-Src	breast:	n/a	chr20:25388314-25388321 chr20:25388310-25388321 chr20:25388311-25388326 chr20:25388310-25388321 chr20:25388310-25388321 chr20:25388309-25388317 chr20:25388310-25388321
33	POLR2A	chr20:25387893-25389250	SK-N-MC	brain:	n/a	n/a
34	MAX	chr20:25387781-25389098	A549	lung:	n/a	n/a
35	ARID3A	chr20:25387822-25388496	HepG2	liver:	n/a	chr20:25388309-25388317
36	MYBL2	chr20:25387821-25388642	HepG2	liver:	n/a	n/a
37	RELA	chr20:25387717-25389061	GM10847	blood:	n/a	n/a
38	FOXM1	chr20:25387842-25388761	GM12878	blood:	n/a	n/a
39	CREB1	chr20:25387891-25388879	HepG2	liver:	n/a	n/a
40	SIN3AK20	chr20:25387861-25388764	HCT-116	colon:	n/a	n/a
41	JUND	chr20:25387895-25388763	H1-hESC	embryonic stem cell:	n/a	chr20:25387947-25387961 chr20:25388588-25388597 chr20:25388319-25388333
42	HCFC1	chr20:25387723-25388731	Hela-S3	cervix:	n/a	n/a
43	RUNX3	chr20:25387816-25388604	GM12878	blood:	n/a	n/a
44	RELA	chr20:25387794-25389014	GM18505	blood:	n/a	n/a
45	RELA	chr20:25387821-25388573	GM18951	blood:	n/a	n/a
46	MXI1	chr20:25387763-25389073	IMR90	lung:	n/a	n/a
47	POLR2A	chr20:25387893-25388616	SK-N-SH	brain:	n/a	n/a
48	MYC	chr20:25387786-25389038	NB4	blood:	n/a	n/a
49	POLR2A	chr20:25387817-25388792	PBDE	blood:	n/a	n/a
50	POLR2A	chr20:25387731-25389121	GM12891	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:25369196..25373772-chr20:25386901..25390344,6	MCF-7	breast:
2	chr20:25385575..25388779-chr20:25393238..25395970,3	K562	blood:

Variant related genes	Relation type
GINS1	TF binding region
ENSG00000100997	Chromatin interaction
ENSG00000101003	Chromatin interaction

Extended variants
information (count: 136 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs1609701	1.00[ASN][1000 genomes]
rs1888038	1.00[ASN][1000 genomes]
rs2039400	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2210053	1.00[ASN][1000 genomes]
rs2258671	1.00[AMR][1000 genomes]
rs2258672	1.00[AMR][1000 genomes]
rs242122	1.00[ASN][1000 genomes]
rs242124	1.00[ASN][1000 genomes]
rs242125	1.00[ASN][1000 genomes]
rs242134	1.00[ASN][1000 genomes]
rs2474768	1.00[AMR][1000 genomes]
rs2474770	1.00[AMR][1000 genomes]
rs2474772	1.00[AMR][1000 genomes]
rs2474775	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2474776	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482916	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2482917	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482920	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482922	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482925	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482929	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482939	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482942	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2482945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500394	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500396	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2500407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500411	1.00[AMR][1000 genomes]
rs2500412	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500416	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2500419	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2500428	1.00[ASN][1000 genomes]
rs2500429	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500431	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500434	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500435	1.00[ASN][1000 genomes]
rs2500437	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500438	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500440	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500444	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500445	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2500447	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2892407	1.00[ASN][1000 genomes]
rs2983490	1.00[AMR][1000 genomes]
rs2990514	1.00[ASN][1000 genomes]
rs2990515	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3002699	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3002700	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3002703	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs364722	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs366060	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs368636	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs368748	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs371447	1.00[ASN][1000 genomes]
rs378534	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs379538	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs380021	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs384336	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs388007	1.00[ASN][1000 genomes]
rs394798	1.00[ASN][1000 genomes]
rs400916	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs409873	1.00[ASN][1000 genomes]
rs409888	1.00[ASN][1000 genomes]
rs417446	1.00[ASN][1000 genomes]
rs417662	1.00[ASN][1000 genomes]
rs423248	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs426143	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs428801	1.00[ASN][1000 genomes]
rs429120	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs432403	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs439642	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs442728	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs448212	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs448866	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4815433	1.00[ASN][1000 genomes]
rs4815434	1.00[ASN][1000 genomes]
rs518336	1.00[AMR][1000 genomes]
rs56165312	1.00[ASN][1000 genomes]
rs57450264	1.00[ASN][1000 genomes]
rs59222176	1.00[ASN][1000 genomes]
rs6037089	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6037112	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6037113	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6037119	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6037147	1.00[ASN][1000 genomes]
rs6037155	1.00[ASN][1000 genomes]
rs60483717	1.00[ASN][1000 genomes]
rs6050591	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6050613	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6050618	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6050627	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6050628	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6050695	1.00[ASN][1000 genomes]
rs6076360	1.00[ASN][1000 genomes]
rs6076365	1.00[ASN][1000 genomes]
rs6083882	1.00[ASN][1000 genomes]
rs6083883	1.00[ASN][1000 genomes]
rs6083887	1.00[ASN][1000 genomes]
rs6115206	1.00[ASN][1000 genomes]
rs6132844	1.00[ASN][1000 genomes]
rs7263728	1.00[ASN][1000 genomes]
rs73904036	1.00[AMR][1000 genomes]
rs73904038	1.00[AMR][1000 genomes]
rs73904039	1.00[AMR][1000 genomes]
rs73904476	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73907308	1.00[ASN][1000 genomes]
rs73907312	1.00[ASN][1000 genomes]
rs73907315	1.00[ASN][1000 genomes]
rs8116049	1.00[ASN][1000 genomes]
rs913790	1.00[ASN][1000 genomes]
rs913791	1.00[ASN][1000 genomes]
rs913793	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063494	chr20:25067286-25468557	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1063016	chr20:25067286-25475629	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS 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	53 gene(s)	inside rSNPs	diseases
3	nsv1065101	chr20:25068046-25466542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv544220	chr20:25068046-25466542	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh 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	53 gene(s)	inside rSNPs	diseases
5	nsv531480	chr20:25070067-25472684	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv585746	chr20:25071454-25470056	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv1062742	chr20:25071454-25475629	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv949389	chr20:25071454-25506582	Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv531481	chr20:25080583-25448944	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv949479	chr20:25096494-25467359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
11	nsv1061109	chr20:25101715-25472685	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv544221	chr20:25101715-25472685	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
13	nsv833948	chr20:25231726-25410540	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS 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	20 gene(s)	inside rSNPs	diseases
14	nsv482647	chr20:25308912-25481982	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription 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	21 gene(s)	inside rSNPs	diseases
15	nsv1056997	chr20:25316663-25492339	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats 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	20 gene(s)	inside rSNPs	diseases
16	nsv1061058	chr20:25327960-25388841	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv1067379	chr20:25355484-25593240	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
18	nsv1061398	chr20:25370106-25444076	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
19	nsv1059494	chr20:25377602-25441835	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25384200-25388000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr20:25384400-25388000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr20:25387600-25388000	Flanking Active TSS	A549	lung
4	chr20:25387600-25388000	Active TSS	HepG2	liver
5	chr20:25387600-25388200	Flanking Active TSS	Dnd41	blood
6	chr20:25387600-25389000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr20:25387600-25389200	Active TSS	GM12878-XiMat	blood
8	chr20:25387600-25389400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:25387800-25388000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr20:25387800-25388000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr20:25387800-25388000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr20:25387800-25388000	Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr20:25387800-25388000	Enhancers	Primary B cells from peripheral blood	blood
14	chr20:25387800-25388000	Active TSS	Primary hematopoietic stem cells	blood
15	chr20:25387800-25388000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr20:25387800-25388000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
17	chr20:25387800-25388000	Active TSS	Liver	Liver
18	chr20:25387800-25388000	Enhancers	Brain Angular Gyrus	brain
19	chr20:25387800-25388000	Enhancers	Brain Hippocampus Middle	brain
20	chr20:25387800-25388000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr20:25387800-25388000	Enhancers	Brain Substantia Nigra	brain
22	chr20:25387800-25388000	Enhancers	Fetal Intestine Small	intestine
23	chr20:25387800-25388000	Active TSS	Fetal Muscle Trunk	muscle
24	chr20:25387800-25388000	Active TSS	Placenta	Placenta
25	chr20:25387800-25388000	Flanking Active TSS	Osteobl	bone
26	chr20:25387800-25388200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr20:25387800-25388200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr20:25387800-25388200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr20:25387800-25388200	Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr20:25387800-25388200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr20:25387800-25388200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr20:25387800-25388200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr20:25387800-25388200	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr20:25387800-25388200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr20:25387800-25388200	Active TSS	Right Atrium	heart
36	chr20:25387800-25388200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr20:25387800-25388200	Active TSS	Stomach Smooth Muscle	stomach
38	chr20:25387800-25388200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr20:25387800-25388200	Flanking Active TSS	NH-A	brain
40	chr20:25387800-25388200	Flanking Active TSS	NHLF	lung
41	chr20:25387800-25388400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr20:25387800-25388400	Enhancers	Fetal Heart	heart
43	chr20:25387800-25388400	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr20:25387800-25388600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr20:25387800-25388600	Active TSS	Primary T cells from cord blood	blood
46	chr20:25387800-25388600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr20:25387800-25388600	Active TSS	Muscle Satellite Cultured Cells	--
48	chr20:25387800-25388600	Active TSS	Brain Anterior Caudate	brain
49	chr20:25387800-25388600	Active TSS	Brain Cingulate Gyrus	brain
50	chr20:25387800-25388600	Active TSS	Colon Smooth Muscle	Colon

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