Variant report

Variant	rs76281250
Chromosome Location	chr20:26188640-26188641
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	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
2	TEAD4	chr20:26188632-26190631	SK-N-SH	brain:	n/a	n/a
3	NFIC	chr20:26188605-26189623	SK-N-SH	brain:	n/a	n/a
4	TAF1	chr20:26188626-26189577	H1-neurons	neurons:	n/a	n/a
5	FOSL2	chr20:26188592-26189574	SK-N-SH	brain:	n/a	chr20:26188722-26188731 chr20:26188715-26188724
6	YY1	chr20:26188627-26189531	SK-N-SH_RA	brain:	n/a	chr20:26189465-26189476 chr20:26188719-26188728 chr20:26189179-26189188 chr20:26188720-26188731
7	EP300	chr20:26188637-26190581	H1-hESC	embryonic stem cell:	n/a	chr20:26188716-26188725 chr20:26189540-26189553
8	BCL3	chr20:26188619-26190737	A549	lung:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
9	POU5F1	chr20:26188511-26189556	H1-hESC	embryonic stem cell:	n/a	n/a
10	SP2	chr20:26188625-26189553	HepG2	liver:	n/a	n/a
11	GABPA	chr20:26188624-26189546	SK-N-SH	brain:	n/a	chr20:26188723-26188732 chr20:26188716-26188725 chr20:26189158-26189167
12	SUZ12	chr20:26188619-26190654	NT2-D1	testis:	n/a	n/a
13	NFIC	chr20:26188592-26189442	ECC-1	luminal epithelium:	n/a	n/a
14	GATA3	chr20:26188634-26189647	A549	lung:	n/a	chr20:26189168-26189175
15	ELF1	chr20:26188620-26190616	SK-N-SH	brain:	n/a	chr20:26188720-26188732 chr20:26189346-26189358 chr20:26190321-26190333
16	YY1	chr20:26188622-26189503	SK-N-SH_RA	brain:	n/a	chr20:26189465-26189476 chr20:26188719-26188728 chr20:26189179-26189188 chr20:26188720-26188731
17	SP4	chr20:26188557-26190728	H1-hESC	embryonic stem cell:	n/a	chr20:26190318-26190334
18	USF2	chr20:26188583-26190668	H1-hESC	embryonic stem cell:	n/a	chr20:26190217-26190233
19	TEAD4	chr20:26188602-26189531	A549	lung:	n/a	n/a
20	MYBL2	chr20:26188573-26189558	HepG2	liver:	n/a	n/a
21	USF1	chr20:26188567-26189521	A549	lung:	n/a	n/a
22	MAX	chr20:26188589-26189595	A549	lung:	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	CEBPB	chr20:26188605-26189629	A549	lung:	n/a	n/a
24	SP4	chr20:26188633-26189524	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr20:26188637-26190747	A549	lung:	n/a	chr20:26190344-26190352
26	POLR2A	chr20:26188636-26189600	H1-neurons	neurons:	n/a	n/a
27	SP2	chr20:26188638-26189527	HepG2	liver:	n/a	n/a
28	JUND	chr20:26188640-26189530	H1-hESC	embryonic stem cell:	n/a	chr20:26188722-26188731 chr20:26188715-26188724
29	EP300	chr20:26188610-26190784	A549	lung:	n/a	chr20:26188716-26188725 chr20:26189540-26189553
30	FOSL2	chr20:26188636-26189593	HepG2	liver:	n/a	chr20:26188722-26188731 chr20:26188715-26188724
31	GABPA	chr20:26188616-26189533	K562	blood:	n/a	chr20:26188723-26188732 chr20:26188716-26188725 chr20:26189158-26189167
32	NRF1	chr20:26188581-26190667	H1-hESC	embryonic stem cell:	n/a	chr20:26188723-26188732 chr20:26188716-26188725 chr20:26189158-26189167
33	TEAD4	chr20:26188527-26189622	A549	lung:	n/a	n/a
34	RXRA	chr20:26188596-26189502	HepG2	liver:	n/a	n/a
35	MAX	chr20:26188575-26189596	A549	lung:	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
36	PAX5	chr20:26188599-26189567	GM12878	blood:	n/a	chr20:26189036-26189063
37	CREB1	chr20:26188625-26189523	A549	lung:	n/a	n/a
38	TCF12	chr20:26188590-26190744	SK-N-SH	brain:	n/a	chr20:26189557-26189567 chr20:26188774-26188784
39	TCF12	chr20:26188586-26189628	ECC-1	luminal epithelium:	n/a	chr20:26189557-26189567 chr20:26188774-26188784
40	SP1	chr20:26188574-26189581	A549	lung:	n/a	n/a
41	ELF1	chr20:26188636-26189517	A549	lung:	n/a	chr20:26188720-26188732 chr20:26189346-26189358
42	MAX	chr20:26188612-26190712	SK-N-SH	brain:	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
43	USF1	chr20:26188569-26189530	A549	lung:	n/a	n/a
44	NR3C1	chr20:26188581-26190553	A549	lung:	n/a	chr20:26189364-26189377 chr20:26190326-26190339
45	MYBL2	chr20:26188621-26189603	HepG2	liver:	n/a	n/a
46	SRF	chr20:26188611-26190565	H1-hESC	embryonic stem cell:	n/a	n/a
47	PML	chr20:26188527-26189550	GM12878	blood:	n/a	chr20:26189407-26189415
48	SIN3AK20	chr20:26188627-26189513	H1-hESC	embryonic stem cell:	n/a	n/a
49	USF1	chr20:26188593-26189523	A549	lung:	n/a	n/a
50	EP300	chr20:26188620-26189504	T-47D	breast:	n/a	chr20:26188716-26188725

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:26188639-26188689	MCF10A-Er-Src	breast:	n/a
2	chr20:26188639-26188689	ProgFib	skin:	n/a
3	chr20:26188639-26188689	AG10803	skin:	n/a
4	chr20:26188639-26188689	HRE	kidney:	n/a
5	chr20:26188639-26188689	GM19239	blood:	n/a
6	chr20:26188639-26188689	NT2-D1	testis:	n/a
7	chr20:26188639-26188689	Caco-2	colon:	n/a
8	chr20:26188639-26188689	AG04449	skin:	fetal
9	chr20:26188639-26188689	HNPCEpiC	eye:	n/a
10	chr20:26188639-26188689	AG09319	gingival:	n/a
11	chr20:26188639-26188689	IMR90	lung:	fetal
12	chr20:26188639-26188689	MCF-7	breast:	n/a
13	chr20:26188639-26188689	U87	brain:	n/a
14	chr20:26188639-26188689	HUVEC	blood vessel:	n/a
15	chr20:26188639-26188689	HEEpiC	esophagus:	n/a
16	chr20:26188639-26188689	NB4	blood:	n/a
17	chr20:26188639-26188689	AG09309	skin:	n/a
18	chr20:26188639-26188689	HL-60	blood:	n/a
19	chr20:26188639-26188689	SK-N-MC	brain:	n/a
20	chr20:26188639-26188689	GM12892	blood:	n/a
21	chr20:26188639-26188689	HepG2	liver:	n/a
22	chr20:26188639-26188689	HCM	heart:	n/a
23	chr20:26188639-26188689	HRCEpiC	kidney:	n/a
24	chr20:26188639-26188689	GM12878	blood:	n/a
25	chr20:26188639-26188689	Jurkat	blood:	n/a
26	chr20:26188639-26188689	K562	blood:	n/a
27	chr20:26188639-26188689	H1-hESC	embryonic stem cell:	embryo
28	chr20:26188639-26188689	BJ	skin:	n/a
29	chr20:26188639-26188689	SK-N-SH_RA	brain:	n/a
30	chr20:26188639-26188689	ovcar-3	ovarian:	n/a
31	chr20:26188639-26188689	GM12891	blood:	n/a
32	chr20:26188639-26188689	HCF	heart:	n/a
33	chr20:26188639-26188689	PrEC	prostate:	n/a
34	chr20:26188639-26188689	ECC-1	luminal epithelium:	n/a
35	chr20:26188639-26188689	HMEC	breast:	n/a
36	chr20:26188639-26188689	RPTEC	kidney:	n/a
37	chr20:26188639-26188689	PFSK-1	brain:	n/a
38	chr20:26188639-26188689	HAEpiC	amniotic membrane:	n/a
39	chr20:26188639-26188689	CMK	blood:	n/a
40	chr20:26188639-26188689	HCPEpiC	choroid plexus:	n/a
41	chr20:26188639-26188689	T-47D	breast:	n/a
42	chr20:26188639-26188689	SAEC	small airway:	n/a
43	chr20:26188639-26188689	SKMC	muscle:	n/a
44	chr20:26188639-26188689	A549	lung:	n/a
45	chr20:26188639-26188689	NHDF-neo	bronchial:	n/a
46	chr20:26188639-26188689	LNCaP	prostate:	n/a
47	chr20:26188639-26188689	BE2_C	brain:	n/a
48	chr20:26188639-26188689	Hela-S3	cervix:	n/a
49	chr20:26188639-26188689	PANC-1	pancreas:	n/a
50	chr20:26188639-26188689	AG04450	lung:	fetal

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	chr20:26187251..26191978-chr21:9823998..9829001,56	K562	blood:
7	chr20:26188413..26189362-chr8:101964386..101965001,2	MCF-7	breast:
8	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:
9	chr2:133011277..133017359-chr20:26187383..26191986,21	K562	blood:
10	chr20:26187273..26191752-chr21:9823988..9828758,49	MCF-7	breast:
11	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
12	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
13	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
14	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:
15	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
16	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
17	chr12:20704427..20705972-chr20:26188595..26190576,2	MCF-7	breast:
18	chr20:26188271..26189555-chr21:9824988..9827433,58	MCF-7	breast:
19	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
20	chr20:26188395..26190565-chr6:74228700..74231505,2	MCF-7	breast:
21	chr12:127649141..127652032-chr20:26188488..26190208,4	K562	blood:
22	chr16:33960780..33961953-chr20:26188513..26190294,8	MCF-7	breast:
23	chr20:26187252..26191975-chr21:9823984..9828995,56	MCF-7	breast:
24	chr20:26188275..26190975-chr21:9824996..9827903,45	K562	blood:
25	chr16:33961325..33966193-chr20:26187372..26191793,13	K562	blood:
26	chr20:26188254..26190671-chr21:9824984..9827890,92	MCF-7	breast:
27	chr12:20703907..20704890-chr20:26188413..26189402,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-6	chr20:26188310-26188679	ENSG00000227195.4
2	lnc-FAM182B-6	chr20:26188310-26188703	ENSG00000227195.4
3	lnc-FAM182B-6	chr20:26188310-26188714	ENSG00000227195.4

Variant related genes	Relation type
MIR663A	TF binding region
MIR663A	CpG island
ENSG00000207986	Chromatin interaction
ENSG00000164924	Chromatin interaction
ENSG00000221288	Chromatin interaction
ENSG00000230102	Chromatin interaction
ENSG00000264063	Chromatin interaction
ENSG00000264462	Chromatin interaction
ENSG00000156508	Chromatin interaction
ENSG00000163046	Chromatin interaction
ENSG00000256663	Chromatin interaction
ENSG00000256642	Chromatin interaction
ENSG00000200434	Chromatin interaction
ENSG00000031698	Chromatin interaction
ENSG00000239776	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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:53 , 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	chr20:26188600-26188800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr20:26188600-26188800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr20:26188600-26188800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr20:26188600-26188800	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
6	chr20:26188600-26188800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
7	chr20:26188600-26188800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
8	chr20:26188600-26188800	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
9	chr20:26188600-26188800	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
10	chr20:26188600-26188800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr20:26188600-26188800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr20:26188600-26188800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
13	chr20:26188600-26188800	Bivalent Enhancer	Aorta	Aorta
14	chr20:26188600-26188800	Bivalent Enhancer	Brain Hippocampus Middle	brain
15	chr20:26188600-26188800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
16	chr20:26188600-26188800	Bivalent/Poised TSS	Fetal Brain Female	brain
17	chr20:26188600-26188800	Bivalent Enhancer	Ovary	ovary
18	chr20:26188600-26188800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
19	chr20:26188600-26189000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
20	chr20:26188600-26189200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
21	chr20:26188600-26189200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr20:26188600-26189200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr20:26188600-26189400	Bivalent Enhancer	Placenta	Placenta
24	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Left Ventricle	heart
25	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Lung	lung
26	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Pancreas	Pancrea
27	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
28	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Right Ventricle	heart
29	chr20:26188600-26189400	Flanking Bivalent TSS/Enh	Spleen	Spleen
30	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
31	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
34	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
35	chr20:26188600-26189600	Flanking Bivalent TSS/Enh	Gastric	stomach
36	chr20:26188600-26190400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
37	chr20:26188600-26190400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr20:26188600-26190400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
39	chr20:26188600-26190400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
40	chr20:26188600-26190400	ZNF genes & repeats	Esophagus	oesophagus
41	chr20:26188600-26190400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
42	chr20:26188600-26190400	ZNF genes & repeats	Dnd41	blood
43	chr20:26188600-26190400	ZNF genes & repeats	NHLF	lung
44	chr20:26188600-26190600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr20:26188600-26190600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
46	chr20:26188600-26190600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
47	chr20:26188600-26190600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr20:26188600-26190600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
49	chr20:26188600-26190600	ZNF genes & repeats	Fetal Intestine Small	intestine
50	chr20:26188600-26190600	ZNF genes & repeats	Fetal Stomach	stomach

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