Variant report

Variant	esv3351059
Chromosome Location	chr11:17739776-17744374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:1161)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:17741849-17741864	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:17740034-17740383	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:17743740-17743870	K562	blood:	n/a	n/a
4	BACH1	chr11:17743545-17743911	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr11:17741781-17741867	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:17741618-17741818	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:17743677-17743912	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:17741695-17741950	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr11:17741837-17741948	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr11:17740541-17740608	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr11:17741176-17742219	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr11:17741391-17743044	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:17743731-17743793	GM10266	blood:	n/a	n/a
14	CTCF	chr11:17743740-17743890	GM12874	blood:	n/a	n/a
15	CTCF	chr11:17742140-17742290	HUVEC	blood vessel:	n/a	chr11:17742240-17742250
16	CTCF	chr11:17743660-17743810	GM12871	blood:	n/a	n/a
17	CTCF	chr11:17743760-17743910	GM12864	blood:	n/a	n/a
18	CTCF	chr11:17741760-17741910	BE2_C	brain:	n/a	n/a
19	CTCF	chr11:17741710-17742274	IMR90	lung:	n/a	chr11:17742240-17742250
20	CTCF	chr11:17742360-17742510	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr11:17741720-17741870	AG04449	skin:	n/a	n/a
22	CTCF	chr11:17742360-17742510	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr11:17741730-17741953	Medullo	brain:	n/a	n/a
24	CTCF	chr11:17741742-17741941	ProgFib	skin:	n/a	n/a
25	CTCF	chr11:17741660-17741810	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr11:17743689-17743845	GM12891	blood:	n/a	n/a
27	CTCF	chr11:17742040-17742190	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr11:17742060-17742210	BJ	skin:	n/a	n/a
29	CTCF	chr11:17741760-17741910	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr11:17743734-17743814	Lung_OC	lung:	n/a	n/a
31	CTCF	chr11:17743740-17743890	GM12875	blood:	n/a	n/a
32	CTCF	chr11:17743720-17743870	GM12864	blood:	n/a	n/a
33	CTCF	chr11:17741780-17741930	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr11:17743898-17743899	LNCaP	prostate:	n/a	n/a
35	CTCF	chr11:17742121-17742168	GM12892	blood:	n/a	n/a
36	CTCF	chr11:17743653-17743869	A549	lung:	n/a	n/a
37	CTCF	chr11:17741740-17741890	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr11:17741668-17741689	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:17742115-17742197	Fibrobl	skin:	n/a	n/a
40	CTCF	chr11:17742760-17742910	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr11:17743574-17743949	K562	blood:	n/a	n/a
42	CTCF	chr11:17743720-17743870	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr11:17743680-17743840	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr11:17743569-17743850	A549	lung:	n/a	n/a
45	CTCF	chr11:17743655-17743924	A549	lung:	n/a	n/a
46	CTCF	chr11:17743732-17743857	GM12878	blood:	n/a	n/a
47	CTCF	chr11:17743653-17743917	Medullo	brain:	n/a	n/a
48	CTCF	chr11:17742340-17742490	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:17743660-17743810	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr11:17742071-17742235	HepG2	liver:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17743667-17743717	Hepatocyte	liver:	n/a
2	chr11:17741925-17741975	HL-60	blood:	n/a
3	chr11:17743667-17743717	Hepatocyte	liver:	n/a
4	chr11:17741925-17741975	HL-60	blood:	n/a
5	chr11:17743840-17743890	MCF-7	breast:	n/a
6	chr11:17740887-17740937	BJ	skin:	n/a
7	chr11:17743667-17743717	HIPEpiC	eye:	n/a
8	chr11:17742759-17742809	SK-N-SH_RA	brain:	n/a
9	chr11:17742135-17742185	CMK	blood:	n/a
10	chr11:17742759-17742809	MCF10A-Er-Src	breast:	n/a
11	chr11:17742759-17742809	NH-A	brain:	n/a
12	chr11:17741687-17741737	Hela-S3	cervix:	n/a
13	chr11:17743840-17743890	A549	lung:	n/a
14	chr11:17743761-17743811	Jurkat	blood:	n/a
15	chr11:17743080-17743130	HUVEC	blood vessel:	n/a
16	chr11:17742741-17742791	HEK293	kidney:	embryo
17	chr11:17741243-17741293	HCPEpiC	choroid plexus:	n/a
18	chr11:17740977-17741027	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:17740977-17741027	HAEpiC	amniotic membrane:	n/a
20	chr11:17742502-17742552	GM12878	blood:	n/a
21	chr11:17741925-17741975	AG09309	skin:	n/a
22	chr11:17743282-17743332	NT2-D1	testis:	n/a
23	chr11:17740967-17741017	HUVEC	blood vessel:	n/a
24	chr11:17743282-17743332	HEK293	kidney:	embryo
25	chr11:17743667-17743717	K562	blood:	n/a
26	chr11:17743610-17743660	HCF	heart:	n/a
27	chr11:17743761-17743811	ProgFib	skin:	n/a
28	chr11:17740967-17741017	HNPCEpiC	eye:	n/a
29	chr11:17742502-17742552	AG09309	skin:	n/a
30	chr11:17743840-17743890	CMK	blood:	n/a
31	chr11:17740967-17741017	HAEpiC	amniotic membrane:	n/a
32	chr11:17743080-17743130	GM12891	blood:	n/a
33	chr11:17742502-17742552	A549	lung:	n/a
34	chr11:17742502-17742552	U87	brain:	n/a
35	chr11:17741687-17741737	PFSK-1	brain:	n/a
36	chr11:17743610-17743660	SKMC	muscle:	n/a
37	chr11:17741243-17741293	AG04449	skin:	fetal
38	chr11:17742502-17742552	HEK293	kidney:	embryo
39	chr11:17740977-17741027	Caco-2	colon:	n/a
40	chr11:17741925-17741975	Hela-S3	cervix:	n/a
41	chr11:17743610-17743660	Jurkat	blood:	n/a
42	chr11:17742759-17742809	HepG2	liver:	n/a
43	chr11:17743761-17743811	NT2-D1	testis:	n/a
44	chr11:17741687-17741737	HepG2	liver:	n/a
45	chr11:17742759-17742809	SK-N-SH	brain:	n/a
46	chr11:17741687-17741737	H1-hESC	embryonic stem cell:	embryo
47	chr11:17740887-17740937	GM06990	blood:	n/a
48	chr11:17740887-17740937	SK-N-SH_RA	brain:	n/a
49	chr11:17743080-17743130	U87	brain:	n/a
50	chr11:17743282-17743332	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:17622678..17623570-chr11:17743313..17743816,2	MCF-7	breast:
2	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
3	chr11:17619891..17621109-chr11:17743288..17744431,5	MCF-7	breast:
4	chr11:17620217..17621179-chr11:17742829..17744247,6	MCF-7	breast:

No data

Variant related genes	Relation type
MYOD1	TF binding region
MYOD1	CpG island

Extended variants
information (count: 215 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:215 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61880589	chr11:17739849-17739850	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs148963505	chr11:17739857-17739858	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528852926	chr11:17739929-17739930	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547378263	chr11:17739960-17739961	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs147065908	chr11:17739996-17739997	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs186593779	chr11:17740078-17740079	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs138263971	chr11:17740147-17740148	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs570645395	chr11:17740173-17740174	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537965213	chr11:17740176-17740177	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs556211612	chr11:17740180-17740181	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12272145	chr11:17740186-17740187	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528866589	chr11:17740188-17740189	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561127408	chr11:17740206-17740207	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs2526549	chr11:17740221-17740222	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2734557	chr11:17740223-17740224	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547042186	chr11:17740255-17740256	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs375834966	chr11:17740266-17740267	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs542164143	chr11:17740271-17740272	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7121212	chr11:17740272-17740273	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143834338	chr11:17740285-17740286	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546109949	chr11:17740290-17740291	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372286369	chr11:17740294-17740295	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs146893008	chr11:17740345-17740346	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs190952858	chr11:17740397-17740398	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533088381	chr11:17740441-17740442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs551269608	chr11:17740453-17740454	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs541537576	chr11:17740478-17740479	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs543566749	chr11:17740501-17740502	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs561719388	chr11:17740526-17740527	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs540493656	chr11:17740557-17740558	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547361218	chr11:17740649-17740650	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs565884187	chr11:17740706-17740707	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183165427	chr11:17740727-17740728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551226104	chr11:17740764-17740765	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs3911833	chr11:17740778-17740779	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536803487	chr11:17740793-17740794	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556246303	chr11:17740795-17740796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568529956	chr11:17740848-17740849	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535525358	chr11:17740855-17740856	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs113564734	chr11:17740896-17740897	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs554116912	chr11:17740910-17740911	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs572686050	chr11:17740942-17740943	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532405459	chr11:17740944-17740945	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs139391382	chr11:17740968-17740969	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs112773749	chr11:17740983-17740984	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs148845207	chr11:17740991-17740992	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs59789883	chr11:17740992-17740993	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs397742305	chr11:17740998-17740999	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs2734548	chr11:17741011-17741012	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs374670186	chr11:17741015-17741016	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17736800-17739800	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr11:17736800-17740400	Weak transcription	Psoas Muscle	Psoas
3	chr11:17736800-17740400	Weak transcription	HSMM	muscle
4	chr11:17736800-17740600	Weak transcription	HSMMtube	muscle
5	chr11:17736800-17741000	Weak transcription	Right Atrium	heart
6	chr11:17739000-17739800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr11:17739200-17740400	Bivalent Enhancer	Fetal Muscle Leg	muscle
8	chr11:17739600-17740000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr11:17739800-17740000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
10	chr11:17739800-17740200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:17739800-17740200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr11:17739800-17740600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr11:17740000-17740200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr11:17740000-17740400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr11:17740000-17740800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
16	chr11:17740200-17740400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
17	chr11:17740200-17740400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
18	chr11:17740200-17740600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:17740200-17740600	Bivalent Enhancer	Placenta	Placenta
20	chr11:17740200-17740800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
21	chr11:17740200-17740800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
22	chr11:17740200-17740800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
23	chr11:17740200-17740800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:17740200-17740800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:17740200-17740800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
26	chr11:17740200-17741400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
27	chr11:17740200-17742000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
28	chr11:17740200-17742600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr11:17740200-17743000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr11:17740200-17743200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
31	chr11:17740200-17743200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr11:17740200-17743600	Bivalent Enhancer	Fetal Heart	heart
33	chr11:17740200-17743800	Bivalent Enhancer	Liver	Liver
34	chr11:17740400-17740600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:17740400-17740600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr11:17740400-17740600	Bivalent Enhancer	Esophagus	oesophagus
37	chr11:17740400-17740600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
38	chr11:17740400-17740600	Bivalent Enhancer	Left Ventricle	heart
39	chr11:17740400-17740800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr11:17740400-17740800	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
41	chr11:17740400-17740800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:17740400-17740800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr11:17740400-17740800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
44	chr11:17740400-17741400	Bivalent/Poised TSS	Right Ventricle	heart
45	chr11:17740400-17743200	Active TSS	Psoas Muscle	Psoas
46	chr11:17740400-17743400	Active TSS	HSMM	muscle
47	chr11:17740600-17740800	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:17740600-17740800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:17740600-17740800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
50	chr11:17740600-17740800	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--

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