Variant report

Variant	esv3404280
Chromosome Location	chr11:9111401-9114249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:855)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:38 , 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	chr11:9112780-9112930	AG04449	skin:	n/a	n/a
3	CTCF	chr11:9114080-9114230	GM06990	blood:	n/a	n/a
4	CTCF	chr11:9113700-9113850	HAc	cerebellar:	n/a	n/a
5	CTCF	chr11:9112420-9112570	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr11:9112320-9112470	HUVEC	blood vessel:	n/a	n/a
7	E2F6	chr11:9112327-9112838	H1-hESC	embryonic stem cell:	n/a	chr11:9112594-9112608 chr11:9112703-9112715
8	E2F6	chr11:9112438-9112898	H1-hESC	embryonic stem cell:	n/a	chr11:9112594-9112608 chr11:9112703-9112715
9	GABPA	chr11:9112541-9112930	H1-hESC	embryonic stem cell:	n/a	chr11:9112848-9112857
10	GATA3	chr11:9110789-9111704	MCF-7	breast:	n/a	n/a
11	GATA3	chr11:9111213-9111503	MCF-7	breast:	n/a	n/a
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	chr11:9111132-9111615	MCF-7	breast:	n/a	n/a
16	MAX	chr11:9112411-9113099	H1-hESC	embryonic stem cell:	n/a	n/a
17	MXI1	chr11:9111003-9111780	SK-N-SH	brain:	n/a	n/a
18	MYC	chr11:9113288-9113425	MCF-7	breast:	n/a	n/a
19	MYC	chr11:9111433-9111475	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr11:9111235-9111438	MCF-7	breast:	n/a	n/a
21	MYC	chr11:9111385-9111449	MCF-7	breast:	n/a	n/a
22	MYC	chr11:9111175-9111512	MCF-7	breast:	n/a	n/a
23	POLR2A	chr11:9111237-9111676	MCF-7	breast:	n/a	n/a
24	POLR2A	chr11:9113278-9113464	MCF-7	breast:	n/a	n/a
25	POLR2A	chr11:9110693-9111955	MCF-7	breast:	n/a	n/a
26	POLR2A	chr11:9112668-9113113	MCF-7	breast:	n/a	n/a
27	POLR2A	chr11:9112892-9113203	MCF-7	breast:	n/a	n/a
28	POLR2A	chr11:9111845-9111861	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:9112884-9112970	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:9111146-9111777	MCF-7	breast:	n/a	n/a
31	POLR2A	chr11:9113239-9113272	MCF-7	breast:	n/a	n/a
32	POLR2A	chr11:9111722-9111802	H1-hESC	embryonic stem cell:	n/a	n/a
33	SIN3A	chr11:9112428-9112704	H1-hESC	embryonic stem cell:	n/a	n/a
34	SIN3A	chr11:9113312-9113560	H1-hESC	embryonic stem cell:	n/a	n/a
35	SIN3A	chr11:9112932-9113097	H1-hESC	embryonic stem cell:	n/a	n/a
36	SIN3AK20	chr11:9110994-9111623	MCF-7	breast:	n/a	n/a
37	ZBTB7A	chr11:9112543-9113924	ECC-1	luminal epithelium:	n/a	chr11:9113313-9113322
38	ZBTB7A	chr11:9112678-9113181	ECC-1	luminal epithelium:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9113167-9113217	GM19239	blood:	n/a
2	chr11:9113167-9113217	GM19239	blood:	n/a
3	chr11:9113406-9113456	HRCEpiC	kidney:	n/a
4	chr11:9113458-9113508	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:9113370-9113420	HL-60	blood:	n/a
6	chr11:9112214-9112264	HNPCEpiC	eye:	n/a
7	chr11:9112214-9112264	AoSMC	blood vessel:	n/a
8	chr11:9113370-9113420	AG10803	skin:	n/a
9	chr11:9113458-9113508	Caco-2	colon:	n/a
10	chr11:9112989-9113039	NHDF-neo	bronchial:	n/a
11	chr11:9113146-9113196	BE2_C	brain:	n/a
12	chr11:9113167-9113217	ovcar-3	ovarian:	n/a
13	chr11:9112214-9112264	HepG2	liver:	n/a
14	chr11:9113152-9113202	HL-60	blood:	n/a
15	chr11:9113458-9113508	LNCaP	prostate:	n/a
16	chr11:9113167-9113217	NH-A	brain:	n/a
17	chr11:9113406-9113456	PrEC	prostate:	n/a
18	chr11:9113167-9113217	GM12878	blood:	n/a
19	chr11:9113406-9113456	MCF10A-Er-Src	breast:	n/a
20	chr11:9112471-9112521	HEEpiC	esophagus:	n/a
21	chr11:9112989-9113039	SK-N-SH_RA	brain:	n/a
22	chr11:9113458-9113508	PrEC	prostate:	n/a
23	chr11:9113190-9113240	HL-60	blood:	n/a
24	chr11:9113184-9113234	HAEpiC	amniotic membrane:	n/a
25	chr11:9113370-9113420	HCM	heart:	n/a
26	chr11:9113179-9113229	BE2_C	brain:	n/a
27	chr11:9113370-9113420	ECC-1	luminal epithelium:	n/a
28	chr11:9113458-9113508	BJ	skin:	n/a
29	chr11:9113184-9113234	MCF10A-Er-Src	breast:	n/a
30	chr11:9113179-9113229	HRCEpiC	kidney:	n/a
31	chr11:9112214-9112264	GM12878	blood:	n/a
32	chr11:9113184-9113234	NT2-D1	testis:	n/a
33	chr11:9113194-9113244	NT2-D1	testis:	n/a
34	chr11:9113194-9113244	T-47D	breast:	n/a
35	chr11:9112989-9113039	HCM	heart:	n/a
36	chr11:9112471-9112521	ECC-1	luminal epithelium:	n/a
37	chr11:9113146-9113196	H1-hESC	embryonic stem cell:	embryo
38	chr11:9113179-9113229	HMEC	breast:	n/a
39	chr11:9113370-9113420	NT2-D1	testis:	n/a
40	chr11:9112214-9112264	A549	lung:	n/a
41	chr11:9113184-9113234	Caco-2	colon:	n/a
42	chr11:9113190-9113240	HUVEC	blood vessel:	n/a
43	chr11:9112989-9113039	HUVEC	blood vessel:	n/a
44	chr11:9113370-9113420	HRPEpiC	eye:	n/a
45	chr11:9113152-9113202	CMK	blood:	n/a
46	chr11:9113152-9113202	U87	brain:	n/a
47	chr11:9113194-9113244	SKMC	muscle:	n/a
48	chr11:9113406-9113456	NT2-D1	testis:	n/a
49	chr11:9112715-9112765	BJ	skin:	n/a
50	chr11:9113184-9113234	Jurkat	blood:	n/a

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

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

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5691	chr11:9111897-9111918	MIMAT0022483

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
ENSG00000166483	chromatin interactions
ENSG00000165527	chromatin interactions
ENSG00000213538	chromatin interactions
ENSG00000175356	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367793405	chr11:9111406-9111407	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs371068962	chr11:9111407-9111408	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs374325007	chr11:9111419-9111420	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs188043472	chr11:9111436-9111437	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs191252612	chr11:9111437-9111438	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs148492581	chr11:9111491-9111492	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs72549214	chr11:9111511-9111512	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs183779879	chr11:9111539-9111540	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs547563719	chr11:9111555-9111556	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs963167	chr11:9111558-9111559	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
11	rs535834722	chr11:9111578-9111579	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs556130371	chr11:9111597-9111598	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs142676778	chr11:9111691-9111692	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs538962538	chr11:9111768-9111769	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs549010061	chr11:9111817-9111818	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs73412019	chr11:9111843-9111844	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs572335129	chr11:9111888-9111889	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs112511786	chr11:9111905-9111906	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region miRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs554804494	chr11:9111908-9111909	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region miRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs574885158	chr11:9111971-9111972	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs375593019	chr11:9111993-9111994	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs188558175	chr11:9112008-9112009	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111988048	chr11:9112014-9112015	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192886377	chr11:9112016-9112017	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs72386909	chr11:9112019-9112020	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs7484187	chr11:9112020-9112021	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs28633109	chr11:9112024-9112025	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs534759745	chr11:9112025-9112026	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs71452502	chr11:9112032-9112033	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs111804485	chr11:9112034-9112035	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs372411596	chr11:9112035-9112036	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs377724235	chr11:9112036-9112037	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs200195747	chr11:9112037-9112038	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545354170	chr11:9112038-9112039	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370940162	chr11:9112039-9112040	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs74052398	chr11:9112040-9112041	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs201678323	chr11:9112043-9112044	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs200381165	chr11:9112044-9112045	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs200761987	chr11:9112047-9112048	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547582231	chr11:9112063-9112064	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs2742517	chr11:9112072-9112073	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
42	rs114721144	chr11:9112098-9112099	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs370864333	chr11:9112116-9112117	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs549477782	chr11:9112119-9112120	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	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
46	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
47	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
48	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
49	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
50	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

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:353 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr11:9100400-9111600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr11:9103400-9112400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:9109800-9112400	Weak transcription	Right Atrium	heart
6	chr11:9110200-9111600	Bivalent Enhancer	HepG2	liver
7	chr11:9110400-9111800	Enhancers	Adipose Nuclei	Adipose
8	chr11:9110400-9112200	Bivalent Enhancer	Fetal Intestine Small	intestine
9	chr11:9110600-9111600	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr11:9110600-9112000	Enhancers	Gastric	stomach
11	chr11:9110600-9112200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:9110800-9112200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr11:9110800-9112200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr11:9110800-9112400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:9110800-9112600	Enhancers	Lung	lung
16	chr11:9110800-9112600	Enhancers	Spleen	Spleen
17	chr11:9111000-9112200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr11:9111000-9112200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr11:9111200-9111600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr11:9111200-9111800	Enhancers	Brain Substantia Nigra	brain
21	chr11:9111200-9111800	Bivalent Enhancer	Fetal Brain Female	brain
22	chr11:9111200-9112000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr11:9111200-9112200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:9111200-9112200	Bivalent Enhancer	Fetal Intestine Large	intestine
25	chr11:9111200-9112200	Enhancers	Fetal Lung	lung
26	chr11:9111200-9112400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:9111200-9112400	Enhancers	HMEC	breast
28	chr11:9111400-9111600	Flanking Active TSS	Colonic Mucosa	Colon
29	chr11:9111400-9111600	Enhancers	Colon Smooth Muscle	Colon
30	chr11:9111400-9111600	Enhancers	Duodenum Mucosa	Duodenum
31	chr11:9111400-9111600	Enhancers	Psoas Muscle	Psoas
32	chr11:9111400-9111600	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr11:9111400-9111600	Bivalent Enhancer	Small Intestine	intestine
34	chr11:9111400-9111800	Flanking Active TSS	Pancreas	Pancrea
35	chr11:9111400-9111800	Bivalent Enhancer	NHEK	skin
36	chr11:9111400-9112000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr11:9111400-9113400	Weak transcription	HSMMtube	muscle
38	chr11:9111400-9113800	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr11:9111600-9111800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:9111600-9111800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
41	chr11:9111600-9111800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr11:9111600-9111800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr11:9111600-9111800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
44	chr11:9111600-9111800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
45	chr11:9111600-9111800	Enhancers	Colonic Mucosa	Colon
46	chr11:9111600-9111800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
47	chr11:9111600-9111800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr11:9111600-9112000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr11:9111600-9112000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
50	chr11:9111600-9112000	Enhancers	Stomach Smooth Muscle	stomach

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