Variant report

Variant	esv3451461
Chromosome Location	chr11:9112126-9114374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:856)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr11:9112790-9113069	A549	lung:	n/a	n/a
2	CTCF	chr11:9114080-9114230	GM06990	blood:	n/a	n/a
3	CTCF	chr11:9114320-9114470	GM12873	blood:	n/a	n/a
4	CTCF	chr11:9112320-9112470	HUVEC	blood vessel:	n/a	n/a
5	CTCF	chr11:9112420-9112570	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr11:9112780-9112930	AG04449	skin:	n/a	n/a
7	CTCF	chr11:9113700-9113850	HAc	cerebellar:	n/a	n/a
8	CTCF	chr11:9114365-9115326	SK-N-SH	brain:	n/a	chr11:9114890-9114903
9	E2F6	chr11:9112438-9112898	H1-hESC	embryonic stem cell:	n/a	chr11:9112594-9112608 chr11:9112703-9112715
10	E2F6	chr11:9112327-9112838	H1-hESC	embryonic stem cell:	n/a	chr11:9112594-9112608 chr11:9112703-9112715
11	GABPA	chr11:9112541-9112930	H1-hESC	embryonic stem cell:	n/a	chr11:9112848-9112857
12	GTF2F1	chr11:9112555-9112559	H1-hESC	embryonic stem cell:	n/a	n/a
13	HA-E2F1	chr11:9113248-9113713	MCF-7	breast:	n/a	chr11:9113357-9113367 chr11:9113314-9113323
14	MAX	chr11:9112429-9112884	H1-hESC	embryonic stem cell:	n/a	n/a
15	MAX	chr11:9112411-9113099	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr11:9113288-9113425	MCF-7	breast:	n/a	n/a
17	POLR2A	chr11:9112668-9113113	MCF-7	breast:	n/a	n/a
18	POLR2A	chr11:9112884-9112970	MCF-7	breast:	n/a	n/a
19	POLR2A	chr11:9112892-9113203	MCF-7	breast:	n/a	n/a
20	POLR2A	chr11:9113239-9113272	MCF-7	breast:	n/a	n/a
21	POLR2A	chr11:9113278-9113464	MCF-7	breast:	n/a	n/a
22	SIN3A	chr11:9113312-9113560	H1-hESC	embryonic stem cell:	n/a	n/a
23	SIN3A	chr11:9112428-9112704	H1-hESC	embryonic stem cell:	n/a	n/a
24	SIN3A	chr11:9112932-9113097	H1-hESC	embryonic stem cell:	n/a	n/a
25	ZBTB7A	chr11:9112543-9113924	ECC-1	luminal epithelium:	n/a	chr11:9113313-9113322
26	ZBTB7A	chr11:9112678-9113181	ECC-1	luminal epithelium:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9112471-9112521	GM12891	blood:	n/a
2	chr11:9113167-9113217	RPTEC	kidney:	n/a
3	chr11:9112471-9112521	GM12891	blood:	n/a
4	chr11:9113167-9113217	RPTEC	kidney:	n/a
5	chr11:9113194-9113244	HRPEpiC	eye:	n/a
6	chr11:9112214-9112264	HepG2	liver:	n/a
7	chr11:9113406-9113456	SKMC	muscle:	n/a
8	chr11:9113370-9113420	SK-N-MC	brain:	n/a
9	chr11:9113146-9113196	MCF-7	breast:	n/a
10	chr11:9112989-9113039	NB4	blood:	n/a
11	chr11:9113152-9113202	RPTEC	kidney:	n/a
12	chr11:9112214-9112264	MCF10A-Er-Src	breast:	n/a
13	chr11:9112715-9112765	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:9112989-9113039	PrEC	prostate:	n/a
15	chr11:9113184-9113234	HCT-116	colon:	n/a
16	chr11:9113179-9113229	HEEpiC	esophagus:	n/a
17	chr11:9113458-9113508	IMR90	lung:	fetal
18	chr11:9113146-9113196	HCT-116	colon:	n/a
19	chr11:9112471-9112521	HEK293	kidney:	embryo
20	chr11:9112715-9112765	ovcar-3	ovarian:	n/a
21	chr11:9112715-9112765	NHBE	bronchial:	n/a
22	chr11:9113458-9113508	HIPEpiC	eye:	n/a
23	chr11:9113194-9113244	HRCEpiC	kidney:	n/a
24	chr11:9112471-9112521	HCF	heart:	n/a
25	chr11:9112989-9113039	HEEpiC	esophagus:	n/a
26	chr11:9113152-9113202	SK-N-SH_RA	brain:	n/a
27	chr11:9112214-9112264	PrEC	prostate:	n/a
28	chr11:9112471-9112521	K562	blood:	n/a
29	chr11:9112989-9113039	GM12891	blood:	n/a
30	chr11:9112715-9112765	HCPEpiC	choroid plexus:	n/a
31	chr11:9112989-9113039	GM06990	blood:	n/a
32	chr11:9113152-9113202	GM06990	blood:	n/a
33	chr11:9113167-9113217	CMK	blood:	n/a
34	chr11:9113406-9113456	GM12891	blood:	n/a
35	chr11:9112214-9112264	Hepatocyte	liver:	n/a
36	chr11:9113190-9113240	HIPEpiC	eye:	n/a
37	chr11:9113146-9113196	SK-N-SH_RA	brain:	n/a
38	chr11:9112214-9112264	RPTEC	kidney:	n/a
39	chr11:9113370-9113420	HEEpiC	esophagus:	n/a
40	chr11:9113167-9113217	PFSK-1	brain:	n/a
41	chr11:9113184-9113234	HRE	kidney:	n/a
42	chr11:9113152-9113202	Hela-S3	cervix:	n/a
43	chr11:9112989-9113039	HCF	heart:	n/a
44	chr11:9113184-9113234	HEK293	kidney:	embryo
45	chr11:9112471-9112521	ProgFib	skin:	n/a
46	chr11:9112214-9112264	HCM	heart:	n/a
47	chr11:9113370-9113420	HCPEpiC	choroid plexus:	n/a
48	chr11:9113370-9113420	HepG2	liver:	n/a
49	chr11:9113406-9113456	AG04450	lung:	fetal
50	chr11:9112989-9113039	HL-60	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9108004..9116385-chr11:9156452..9162678,21	MCF-7	breast:
2	chr11:9109700..9116224-chr11:9155740..9163743,14	MCF-7	breast:
3	chr11:9113356..9115182-chr11:9141033..9143763,3	MCF-7	breast:
4	chr11:9114158..9114977-chr11:9142176..9142774,2	MCF-7	breast:
5	chr11:9112943..9114701-chr11:9593377..9596594,3	MCF-7	breast:
6	chr11:9109535..9113708-chr11:9115640..9120311,8	MCF-7	breast:
7	chr11:9110779..9112949-chr14:50359771..50361759,2	MCF-7	breast:

No data

Variant related genes	Relation type
MIR5691	TF binding region
KRT8P41	TF binding region
SCUBE2	TF binding region
MIR5691	CpG island
KRT8P41	CpG island
SCUBE2	CpG island
ENSG00000213538	chromatin interactions
ENSG00000175356	chromatin interactions
ENSG00000166483	chromatin interactions
ENSG00000165527	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372872053	chr11:9112230-9112231	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs145912266	chr11:9112264-9112265	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs538925339	chr11:9112317-9112318	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs147798509	chr11:9112327-9112328	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs565925586	chr11:9112343-9112344	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs115655667	chr11:9112355-9112356	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs556890690	chr11:9112389-9112390	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs577139392	chr11:9112448-9112449	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs141223589	chr11:9112497-9112498	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs113808225	chr11:9112531-9112532	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs137887007	chr11:9112536-9112537	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs546053580	chr11:9112550-9112551	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs545314901	chr11:9112571-9112572	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs74052399	chr11:9112572-9112573	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs112878514	chr11:9112658-9112659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs113196481	chr11:9112685-9112686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs540843725	chr11:9112694-9112695	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs369227853	chr11:9112751-9112752	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs561152183	chr11:9112789-9112790	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs529739224	chr11:9112790-9112791	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs112006375	chr11:9112803-9112804	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs562943474	chr11:9112804-9112805	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532018909	chr11:9112808-9112809	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs551763995	chr11:9112876-9112877	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs375449503	chr11:9112879-9112880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs565985625	chr11:9112882-9112883	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs535349556	chr11:9112923-9112924	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs548456435	chr11:9112958-9112959	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs532141846	chr11:9112985-9112986	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs60494098	chr11:9113002-9113003	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
31	rs142900716	chr11:9113009-9113010	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs537125511	chr11:9113027-9113028	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs59844091	chr11:9113030-9113031	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs557532665	chr11:9113069-9113070	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs577426929	chr11:9113088-9113089	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs539799140	chr11:9113094-9113095	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs553428317	chr11:9113111-9113112	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs7126036	chr11:9113146-9113147	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs541351642	chr11:9113201-9113202	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs560898998	chr11:9113239-9113240	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs574624321	chr11:9113322-9113323	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs181888490	chr11:9113327-9113328	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs372469232	chr11:9113333-9113334	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs563002896	chr11:9113447-9113448	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs532081105	chr11:9113459-9113460	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs149438020	chr11:9113468-9113469	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs7105754	chr11:9113474-9113475	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs77941108	chr11:9113496-9113497	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs376849652	chr11:9113544-9113545	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs548889647	chr11:9113560-9113561	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9088200-9112400	Weak transcription	HSMM	muscle
2	chr11:9099400-9112200	Weak transcription	Fetal Heart	heart
3	chr11:9103400-9112400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:9109800-9112400	Weak transcription	Right Atrium	heart
5	chr11:9110400-9112200	Bivalent Enhancer	Fetal Intestine Small	intestine
6	chr11:9110600-9112200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:9110800-9112200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:9110800-9112200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr11:9110800-9112400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:9110800-9112600	Enhancers	Lung	lung
11	chr11:9110800-9112600	Enhancers	Spleen	Spleen
12	chr11:9111000-9112200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr11:9111000-9112200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr11:9111200-9112200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:9111200-9112200	Bivalent Enhancer	Fetal Intestine Large	intestine
16	chr11:9111200-9112200	Enhancers	Fetal Lung	lung
17	chr11:9111200-9112400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:9111200-9112400	Enhancers	HMEC	breast
19	chr11:9111400-9113400	Weak transcription	HSMMtube	muscle
20	chr11:9111400-9113800	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr11:9111600-9112200	Weak transcription	Colon Smooth Muscle	Colon
22	chr11:9111600-9112400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:9111600-9112400	Weak transcription	Psoas Muscle	Psoas
24	chr11:9111600-9113400	Active TSS	Rectal Smooth Muscle	rectum
25	chr11:9111800-9112200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr11:9111800-9112200	Enhancers	Pancreas	Pancrea
27	chr11:9111800-9112400	Weak transcription	Brain Substantia Nigra	brain
28	chr11:9111800-9112400	Weak transcription	Colonic Mucosa	Colon
29	chr11:9112000-9112200	Enhancers	Adipose Nuclei	Adipose
30	chr11:9112000-9112200	Enhancers	Brain Anterior Caudate	brain
31	chr11:9112000-9112400	Weak transcription	Gastric	stomach
32	chr11:9112000-9112600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:9112000-9112800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
34	chr11:9112000-9112800	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr11:9112000-9113000	Bivalent Enhancer	Fetal Brain Male	brain
36	chr11:9112200-9112400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
37	chr11:9112200-9112400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
38	chr11:9112200-9112400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
39	chr11:9112200-9112400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:9112200-9112400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr11:9112200-9112400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:9112200-9112400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:9112200-9112400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
44	chr11:9112200-9112400	Enhancers	Brain Hippocampus Middle	brain
45	chr11:9112200-9112400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:9112200-9112400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
47	chr11:9112200-9112400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr11:9112200-9112400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
49	chr11:9112200-9112400	Flanking Active TSS	Pancreas	Pancrea
50	chr11:9112200-9112400	Enhancers	HUVEC	blood vessel

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