Variant report

Variant	rs56160519
Chromosome Location	chr20:26189201-26189202
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	YY1	chr20:26188762-26189504	GM12891	blood:	n/a	chr20:26189465-26189476 chr20:26189179-26189188
2	MBD4	chr20:26188732-26189581	HepG2	liver:	n/a	n/a
3	ATF3	chr20:26188754-26189204	K562	blood:	n/a	n/a
4	JUND	chr20:26188582-26190554	A549	lung:	n/a	chr20:26190227-26190236 chr20:26189734-26189743 chr20:26189722-26189731 chr20:26188722-26188731 chr20:26188715-26188724 chr20:26189733-26189742
5	TEAD4	chr20:26188632-26190631	SK-N-SH	brain:	n/a	n/a
6	ZEB1	chr20:26188678-26189511	GM12878	blood:	n/a	chr20:26188775-26188786
7	EP300	chr20:26188660-26189537	GM12878	blood:	n/a	chr20:26188716-26188725
8	FOXA2	chr20:26188646-26189529	HepG2	liver:	n/a	n/a
9	SMC3	chr20:26188665-26190662	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr20:26188664-26190665	HepG2	liver:	n/a	n/a
11	MAFK	chr20:26188676-26190654	HepG2	liver:	n/a	n/a
12	NFIC	chr20:26188605-26189623	SK-N-SH	brain:	n/a	n/a
13	ATF2	chr20:26188742-26189499	GM12878	blood:	n/a	n/a
14	SRF	chr20:26188757-26189215	HepG2	liver:	n/a	n/a
15	FOSL1	chr20:26188662-26189502	K562	blood:	n/a	chr20:26188722-26188731 chr20:26188715-26188724
16	EBF1	chr20:26188667-26190667	GM12878	blood:	n/a	n/a
17	JUN	chr20:26188660-26190667	H1-hESC	embryonic stem cell:	n/a	chr20:26190227-26190236 chr20:26189734-26189743 chr20:26189722-26189731 chr20:26188722-26188731 chr20:26188715-26188724 chr20:26189733-26189742
18	TAF1	chr20:26188626-26189577	H1-neurons	neurons:	n/a	n/a
19	CREB1	chr20:26188760-26189522	K562	blood:	n/a	n/a
20	MAZ	chr20:26188660-26190669	Hela-S3	cervix:	n/a	chr20:26190052-26190062 chr20:26189735-26189745 chr20:26189104-26189114 chr20:26189104-26189115 chr20:26189105-26189114 chr20:26189106-26189113 chr20:26189104-26189115 chr20:26189101-26189116 chr20:26189104-26189113 chr20:26189719-26189729 chr20:26189105-26189115 chr20:26189103-26189116 chr20:26189105-26189114 chr20:26189469-26189479 chr20:26189958-26189968
21	ATF3	chr20:26188643-26190671	A549	lung:	n/a	chr20:26190344-26190352
22	MAX	chr20:26188792-26189488	SK-N-SH	brain:	n/a	chr20:26189104-26189114 chr20:26189104-26189115 chr20:26189105-26189114 chr20:26189106-26189113 chr20:26189104-26189115 chr20:26189101-26189116 chr20:26189104-26189113 chr20:26189105-26189115 chr20:26189103-26189116 chr20:26189105-26189114 chr20:26189469-26189479
23	TAF1	chr20:26188710-26189510	H1-neurons	neurons:	n/a	n/a
24	FOSL2	chr20:26188592-26189574	SK-N-SH	brain:	n/a	chr20:26188722-26188731 chr20:26188715-26188724
25	ATF3	chr20:26188677-26189497	HepG2	liver:	n/a	n/a
26	POLR2A	chr20:26188695-26190645	MCF10A-Er-Src	breast:	n/a	n/a
27	MTA3	chr20:26188745-26189433	GM12878	blood:	n/a	n/a
28	CTCF	chr20:26188762-26189230	Lung_OC	lung:	n/a	n/a
29	TRIM28	chr20:26188660-26189336	K562	blood:	n/a	n/a
30	BCL3	chr20:26188670-26189518	GM12878	blood:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
31	POLR2A	chr20:26188752-26189470	HUVEC	blood vessel:	n/a	n/a
32	PAX5	chr20:26188751-26189508	GM12891	blood:	n/a	chr20:26189036-26189063
33	CTCF	chr20:26189200-26189350	HL-60	blood:	n/a	n/a
34	POLR2A	chr20:26188782-26189447	MCF-7	breast:	n/a	n/a
35	GABPA	chr20:26188732-26189220	K562	blood:	n/a	chr20:26189158-26189167
36	YY1	chr20:26188627-26189531	SK-N-SH_RA	brain:	n/a	chr20:26189465-26189476 chr20:26188719-26188728 chr20:26189179-26189188 chr20:26188720-26188731
37	CEBPD	chr20:26188693-26189541	K562	blood:	n/a	n/a
38	MEF2C	chr20:26188648-26189520	GM12878	blood:	n/a	n/a
39	ARID3A	chr20:26188665-26190661	K562	blood:	n/a	n/a
40	USF1	chr20:26188765-26189218	A549	lung:	n/a	n/a
41	ELK1	chr20:26188664-26190665	K562	blood:	n/a	n/a
42	TCF3	chr20:26188664-26189576	GM12878	blood:	n/a	n/a
43	EP300	chr20:26188637-26190581	H1-hESC	embryonic stem cell:	n/a	chr20:26188716-26188725 chr20:26189540-26189553
44	YY1	chr20:26188768-26189213	HCT-116	colon:	n/a	chr20:26189179-26189188
45	BCL3	chr20:26188619-26190737	A549	lung:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
46	MAX	chr20:26188665-26190645	HUVEC	blood vessel:	n/a	chr20:26190052-26190062 chr20:26189735-26189745 chr20:26189104-26189114 chr20:26189104-26189115 chr20:26189105-26189114 chr20:26189106-26189113 chr20:26189104-26189115 chr20:26189101-26189116 chr20:26189104-26189113 chr20:26189719-26189729 chr20:26189105-26189115 chr20:26189103-26189116 chr20:26189105-26189114 chr20:26189469-26189479 chr20:26189958-26189968
47	RFX5	chr20:26188673-26190666	K562	blood:	n/a	n/a
48	FOXA2	chr20:26188696-26189494	HepG2	liver:	n/a	n/a
49	NR2C2	chr20:26188719-26190637	K562	blood:	n/a	n/a
50	POU5F1	chr20:26188511-26189556	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
2	chr20:26188251..26190477-chr21:9825050..9827838,61	MCF-7	breast:
3	chr20:26188341..26189368-chr21:9825099..9826092,4	MCF-7	breast:
4	chr20:26187350..26191964-chr21:9824053..9828992,54	K562	blood:
5	chr20:26188344..26189679-chr21:9825010..9826530,20	HCT-116	colon:
6	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
7	chr16:33960800..33961892-chr20:26188687..26190008,21	MCF-7	breast:
8	chr20:26187251..26191978-chr21:9823998..9829001,56	K562	blood:
9	chr20:26188413..26189362-chr8:101964386..101965001,2	MCF-7	breast:
10	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:
11	chr2:133011277..133017359-chr20:26187383..26191986,21	K562	blood:
12	chr20:26187273..26191752-chr21:9823988..9828758,49	MCF-7	breast:
13	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
14	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
15	chr20:26189053..26190595-chr8:67624606..67626126,2	MCF-7	breast:
16	chr16:33961305..33961892-chr20:26188839..26189533,2	MCF-7	breast:
17	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
18	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:
19	chr20:26188947..26190833-chr6:26156720..26159562,2	MCF-7	breast:
20	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
21	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
22	chr2:133015237..133015768-chr20:26189161..26190454,3	K562	blood:
23	chr12:20704427..20705972-chr20:26188595..26190576,2	MCF-7	breast:
24	chr20:26188271..26189555-chr21:9824988..9827433,58	MCF-7	breast:
25	chr2:133014727..133015757-chr20:26189158..26190413,12	MCF-7	breast:
26	chr16:33960878..33961871-chr20:26188853..26189656,7	MCF-7	breast:
27	chr18:8406500..8407500-chr20:26188735..26189378,2	MCF-7	breast:
28	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
29	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
30	chr2:133014681..133015764-chr20:26189070..26190458,26	MCF-7	breast:
31	chr20:26188395..26190565-chr6:74228700..74231505,2	MCF-7	breast:
32	chr12:127649141..127652032-chr20:26188488..26190208,4	K562	blood:
33	chr16:33960780..33961953-chr20:26188513..26190294,8	MCF-7	breast:
34	chr20:26187252..26191975-chr21:9823984..9828995,56	MCF-7	breast:
35	chr20:26188275..26190975-chr21:9824996..9827903,45	K562	blood:
36	chr17:73256462..73259302-chr20:26189013..26191624,2	MCF-7	breast:
37	chr16:33961325..33966193-chr20:26187372..26191793,13	K562	blood:
38	chr20:26188254..26190671-chr21:9824984..9827890,92	MCF-7	breast:
39	chr16:33961300..33961956-chr20:26188840..26189578,6	MCF-7	breast:
40	chr12:20703907..20704890-chr20:26188413..26189402,2	MCF-7	breast:
41	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
42	chr16:33964537..33965670-chr20:26188912..26190067,3	K562	blood:
43	chr2:133014738..133015584-chr20:26189167..26190034,2	NB4	blood:

Variant related genes	Relation type
MIR663A	TF binding region
ENSG00000125447	Chromatin interaction
ENSG00000164924	Chromatin interaction
ENSG00000163046	Chromatin interaction
ENSG00000207986	Chromatin interaction
ENSG00000256663	Chromatin interaction
ENSG00000239776	Chromatin interaction
ENSG00000230102	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000104205	Chromatin interaction
ENSG00000125445	Chromatin interaction
ENSG00000221288	Chromatin interaction
ENSG00000264063	Chromatin interaction
ENSG00000264462	Chromatin interaction
ENSG00000156508	Chromatin interaction
ENSG00000256642	Chromatin interaction
ENSG00000031698	Chromatin interaction
ENSG00000200434	Chromatin interaction
ENSG00000263970	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs6051213	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6115563	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6115565	1.00[ASN][1000 genomes]
rs845786	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758517	chr20:25701992-26319569	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
2	esv2758790	chr20:25701992-26319569	Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv470545	chr20:25715507-26309255	Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
4	nsv1060065	chr20:25832105-26305567	Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
5	nsv585761	chr20:25892571-26299677	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	41 gene(s)	inside rSNPs	diseases
6	nsv1060508	chr20:25918612-26305567	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
7	nsv1057970	chr20:25937126-26305567	Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1059447	chr20:25941928-26305567	Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
9	nsv1067411	chr20:25955110-26305567	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
10	nsv1065198	chr20:25959162-26305567	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
11	esv2763226	chr20:26007281-26255704	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
12	nsv1062308	chr20:26080988-26197931	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
13	nsv458955	chr20:26085338-26246086	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
14	nsv458956	chr20:26085338-26246086	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
15	nsv458957	chr20:26085338-26246086	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
16	nsv585771	chr20:26085338-26246086	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
17	nsv585772	chr20:26105414-26271193	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
18	nsv585774	chr20:26106445-26318279	Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
19	nsv482712	chr20:26111091-26279775	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
20	nsv458958	chr20:26115510-26246086	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
21	nsv585775	chr20:26115510-26246086	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
22	nsv428686	chr20:26124000-26233848	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
23	nsv458959	chr20:26146163-26246086	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
24	nsv585776	chr20:26146163-26246086	Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
25	nsv1060178	chr20:26167980-26225145	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
26	esv33036	chr20:26182045-26220912	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
27	nsv9799	chr20:26187878-26191877	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:26188400-26189600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr20:26188600-26189400	Bivalent Enhancer	Placenta	Placenta
3	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Left Ventricle	heart
4	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Lung	lung
5	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Pancreas	Pancrea
6	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
7	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Right Ventricle	heart
8	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Spleen	Spleen
9	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
13	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
14	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Gastric	stomach
15	chr20:26188600-26190400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr20:26188600-26190400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr20:26188600-26190400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
18	chr20:26188600-26190400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
19	chr20:26188600-26190400	ZNF genes & repeats	Esophagus	oesophagus
20	chr20:26188600-26190400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
21	chr20:26188600-26190400	ZNF genes & repeats	Dnd41	blood
22	chr20:26188600-26190400	ZNF genes & repeats	NHLF	lung
23	chr20:26188600-26190600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr20:26188600-26190600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr20:26188600-26190600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr20:26188600-26190600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr20:26188600-26190600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
28	chr20:26188600-26190600	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr20:26188600-26190600	ZNF genes & repeats	Fetal Stomach	stomach
30	chr20:26188600-26190600	ZNF genes & repeats	Right Atrium	heart
31	chr20:26188600-26190600	ZNF genes & repeats	Small Intestine	intestine
32	chr20:26188600-26190600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
33	chr20:26188800-26189400	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr20:26188800-26189400	Transcr. at gene 5' and 3'	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr20:26188800-26189400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr20:26188800-26189400	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr20:26188800-26189400	Flanking Bivalent TSS/Enh	Ovary	ovary
38	chr20:26188800-26189400	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion
39	chr20:26188800-26189400	Flanking Bivalent TSS/Enh	Thymus	Thymus
40	chr20:26188800-26189600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr20:26188800-26189600	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
42	chr20:26188800-26189600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr20:26188800-26189600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
44	chr20:26188800-26189600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
45	chr20:26188800-26189800	Bivalent Enhancer	Fetal Heart	heart
46	chr20:26188800-26190000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr20:26188800-26190200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr20:26188800-26190200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr20:26188800-26190200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
50	chr20:26188800-26190200	ZNF genes & repeats	HUVEC	blood vessel

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