Variant report

Variant	esv3435139
Chromosome Location	chr11:45906376-45908374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:733)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45907028-45907063	K562	blood:	n/a	n/a
2	BACH1	chr11:45906869-45907095	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:45907354-45907385	K562	blood:	n/a	n/a
4	BHLHE40	chr11:45906929-45906996	K562	blood:	n/a	n/a
5	CCNT2	chr11:45906879-45907439	K562	blood:	n/a	n/a
6	CHD1	chr11:45907614-45907995	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr11:45906905-45907370	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr11:45907066-45907073	GM12878	blood:	n/a	n/a
9	CHD2	chr11:45906850-45907147	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr11:45906914-45907108	HepG2	liver:	n/a	n/a
11	CHD2	chr11:45906991-45907114	K562	blood:	n/a	n/a
12	CTCF	chr11:45906940-45907090	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr11:45906840-45906990	HRE	kidney:	n/a	n/a
14	CTCF	chr11:45906940-45907090	Caco-2	colon:	n/a	n/a
15	CTCF	chr11:45906909-45907133	K562	blood:	n/a	n/a
16	CTCF	chr11:45906880-45907030	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr11:45906920-45907070	GM12868	blood:	n/a	n/a
18	CTCF	chr11:45906994-45907077	GM12878	blood:	n/a	n/a
19	CTCF	chr11:45906972-45907063	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:45906800-45906950	HVMF	connective:	n/a	n/a
21	CTCF	chr11:45907001-45907034	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:45906860-45907010	GM12870	blood:	n/a	n/a
23	CTCF	chr11:45906900-45907050	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr11:45906958-45907078	K562	blood:	n/a	n/a
25	CTCF	chr11:45906780-45906930	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr11:45906940-45907090	AG04449	skin:	n/a	n/a
27	CTCF	chr11:45906860-45907010	HCT-116	colon:	n/a	n/a
28	CTCF	chr11:45906840-45906990	BJ	skin:	n/a	n/a
29	CTCF	chr11:45907024-45907044	GM12878	blood:	n/a	n/a
30	CTCF	chr11:45906915-45907092	K562	blood:	n/a	n/a
31	CTCF	chr11:45907720-45907870	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr11:45906820-45906970	GM12874	blood:	n/a	n/a
33	CTCF	chr11:45906923-45907064	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr11:45906920-45907070	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr11:45906989-45907053	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr11:45906880-45907030	AG09319	gingival:	n/a	n/a
37	CTCF	chr11:45906880-45907030	K562	blood:	n/a	n/a
38	CTCF	chr11:45906913-45907076	GM10248	blood:	n/a	n/a
39	CTCF	chr11:45907014-45907020	GM12878	blood:	n/a	n/a
40	CTCF	chr11:45906980-45907130	K562	blood:	n/a	n/a
41	CTCF	chr11:45906984-45907051	MCF-7	breast:	n/a	n/a
42	CTCF	chr11:45906812-45907088	K562	blood:	n/a	n/a
43	CTCF	chr11:45906995-45907027	GM12891	blood:	n/a	n/a
44	CTCF	chr11:45906948-45907088	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:45906960-45907076	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr11:45906950-45906960	GM13977	blood:	n/a	n/a
47	CUX1	chr11:45906850-45907005	K562	blood:	n/a	n/a
48	E2F4	chr11:45907291-45907333	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr11:45907149-45907398	GM12878	blood:	n/a	n/a
50	EGR1	chr11:45906962-45907147	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45906914-45906964	HMEC	breast:	n/a
2	chr11:45906914-45906964	HMEC	breast:	n/a
3	chr11:45907069-45907119	HAEpiC	amniotic membrane:	n/a
4	chr11:45908036-45908086	H1-hESC	embryonic stem cell:	embryo
5	chr11:45907147-45907197	AoSMC	blood vessel:	n/a
6	chr11:45906625-45906675	GM12892	blood:	n/a
7	chr11:45907071-45907121	Caco-2	colon:	n/a
8	chr11:45907071-45907121	NT2-D1	testis:	n/a
9	chr11:45908036-45908086	K562	blood:	n/a
10	chr11:45908036-45908086	PFSK-1	brain:	n/a
11	chr11:45906499-45906549	GM12891	blood:	n/a
12	chr11:45907078-45907128	HIPEpiC	eye:	n/a
13	chr11:45907071-45907121	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:45907071-45907121	AG09309	skin:	n/a
15	chr11:45907154-45907204	SKMC	muscle:	n/a
16	chr11:45907412-45907462	GM19239	blood:	n/a
17	chr11:45907808-45907858	CMK	blood:	n/a
18	chr11:45907071-45907121	HAEpiC	amniotic membrane:	n/a
19	chr11:45906499-45906549	Caco-2	colon:	n/a
20	chr11:45906914-45906964	AG04449	skin:	fetal
21	chr11:45907154-45907204	NHDF-neo	bronchial:	n/a
22	chr11:45906625-45906675	HNPCEpiC	eye:	n/a
23	chr11:45906499-45906549	PANC-1	pancreas:	n/a
24	chr11:45906625-45906675	SAEC	small airway:	n/a
25	chr11:45906625-45906675	K562	blood:	n/a
26	chr11:45907147-45907197	BJ	skin:	n/a
27	chr11:45908036-45908086	HEK293	kidney:	embryo
28	chr11:45907500-45907550	RPTEC	kidney:	n/a
29	chr11:45908036-45908086	HEEpiC	esophagus:	n/a
30	chr11:45907412-45907462	NHDF-neo	bronchial:	n/a
31	chr11:45907078-45907128	AG04450	lung:	fetal
32	chr11:45907147-45907197	GM12891	blood:	n/a
33	chr11:45906499-45906549	AG04450	lung:	fetal
34	chr11:45907808-45907858	GM19239	blood:	n/a
35	chr11:45907808-45907858	HMEC	breast:	n/a
36	chr11:45907078-45907128	NHBE	bronchial:	n/a
37	chr11:45907412-45907462	NB4	blood:	n/a
38	chr11:45908036-45908086	AG09319	gingival:	n/a
39	chr11:45907154-45907204	NT2-D1	testis:	n/a
40	chr11:45907154-45907204	HCM	heart:	n/a
41	chr11:45906625-45906675	GM06990	blood:	n/a
42	chr11:45906625-45906675	HEEpiC	esophagus:	n/a
43	chr11:45907154-45907204	HIPEpiC	eye:	n/a
44	chr11:45907412-45907462	H1-hESC	embryonic stem cell:	embryo
45	chr11:45906625-45906675	CMK	blood:	n/a
46	chr11:45907069-45907119	GM06990	blood:	n/a
47	chr11:45907500-45907550	SKMC	muscle:	n/a
48	chr11:45907069-45907119	HCT-116	colon:	n/a
49	chr11:45907808-45907858	HRCEpiC	kidney:	n/a
50	chr11:45907154-45907204	HEEpiC	esophagus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45888702..45891057-chr11:45904911..45907023,2	MCF-7	breast:
2	chr11:45904585..45907305-chr11:45939491..45941669,2	K562	blood:
3	chr11:45868680..45870553-chr11:45907106..45909020,2	K562	blood:
4	chr11:45905425..45907108-chr11:45954120..45957048,2	K562	blood:
5	chr11:45907661..45910600-chr11:45912657..45914797,3	MCF-7	breast:
6	chr11:45892807..45894535-chr11:45907209..45909004,2	K562	blood:
7	chr11:45904326..45907019-chr11:45920750..45923690,3	MCF-7	breast:
8	chr11:45868641..45870553-chr11:45905537..45909020,4	K562	blood:
9	chr11:45867854..45870393-chr11:45906869..45909551,2	MCF-7	breast:
10	chr11:45907546..45909448-chr11:45934193..45936568,2	MCF-7	breast:
11	chr11:45906755..45908288-chr11:45937921..45939853,2	MCF-7	breast:
12	chr11:45869438..45872196-chr11:45903876..45906831,3	K562	blood:
13	chr11:45904574..45907083-chr11:45920026..45922634,2	MCF-7	breast:
14	chr11:45904999..45908778-chr11:45926674..45929138,4	MCF-7	breast:

No data

Variant related genes	Relation type
MAPK8IP1	TF binding region
MAPK8IP1	CpG island
ENSG00000234776	chromatin interactions
ENSG00000255498	chromatin interactions
ENSG00000121653	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000121671	chromatin interactions

Extended variants
information (count: 43 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189652060	chr11:45906416-45906417	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs112225736	chr11:45906419-45906420	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs139988409	chr11:45906432-45906433	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs192157263	chr11:45906491-45906492	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs386753191	chr11:45906493-45906494	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs116140878	chr11:45906494-45906495	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs551471261	chr11:45906495-45906496	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs571379030	chr11:45906496-45906497	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs537001857	chr11:45906684-45906685	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs542982007	chr11:45906706-45906707	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs556995720	chr11:45906735-45906736	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs573628904	chr11:45906740-45906741	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs536147050	chr11:45906764-45906765	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs185735973	chr11:45906771-45906772	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs572928271	chr11:45906800-45906801	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs1554338	chr11:45906830-45906831	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564999702	chr11:45906840-45906841	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs377508761	chr11:45906881-45906882	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs544346413	chr11:45906892-45906893	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs528519464	chr11:45906897-45906898	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs561120163	chr11:45906939-45906940	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs530144680	chr11:45907098-45907099	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs546957677	chr11:45907106-45907107	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs371004601	chr11:45907301-45907302	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs111751468	chr11:45907367-45907368	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs532716851	chr11:45907380-45907381	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs201511756	chr11:45907402-45907403	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs552811406	chr11:45907403-45907404	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs571313860	chr11:45907415-45907416	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs374024490	chr11:45907610-45907611	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs1980218	chr11:45907742-45907743	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190248672	chr11:45907763-45907764	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs143859172	chr11:45907816-45907817	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs181609819	chr11:45907879-45907880	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs185979460	chr11:45907905-45907906	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs566769894	chr11:45907978-45907979	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs530931666	chr11:45908021-45908022	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs538400350	chr11:45908029-45908030	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs558328142	chr11:45908054-45908055	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs146874725	chr11:45908094-45908095	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs188883010	chr11:45908099-45908100	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs376150528	chr11:45908181-45908182	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs555076635	chr11:45908364-45908365	Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45885800-45906400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:45893000-45906800	Weak transcription	HSMM	muscle
3	chr11:45893200-45906600	Weak transcription	Small Intestine	intestine
4	chr11:45895000-45907200	Weak transcription	HUVEC	blood vessel
5	chr11:45895400-45906800	Weak transcription	NH-A	brain
6	chr11:45898600-45906600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr11:45898600-45906800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:45898600-45906800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:45898800-45906400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr11:45898800-45906800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:45898800-45907200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:45899400-45906600	Weak transcription	GM12878-XiMat	blood
13	chr11:45899800-45906600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr11:45900200-45906800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:45900400-45906600	Weak transcription	HepG2	liver
16	chr11:45901400-45906600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr11:45901800-45906600	Strong transcription	Fetal Intestine Small	intestine
18	chr11:45901800-45906800	Weak transcription	NHEK	skin
19	chr11:45902200-45906600	Weak transcription	Hela-S3	cervix
20	chr11:45902200-45906800	Weak transcription	HMEC	breast
21	chr11:45902400-45906800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr11:45902600-45906800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:45902800-45906600	Weak transcription	Fetal Brain Male	brain
24	chr11:45902800-45906800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:45902800-45907000	Weak transcription	Psoas Muscle	Psoas
26	chr11:45903000-45906600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr11:45903000-45906600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr11:45903000-45906600	Weak transcription	Fetal Lung	lung
29	chr11:45903200-45907200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:45903200-45907200	Weak transcription	NHDF-Ad	bronchial
31	chr11:45903400-45906400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr11:45903400-45906600	Weak transcription	Stomach Mucosa	stomach
33	chr11:45903400-45906800	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr11:45903400-45906800	Weak transcription	A549	lung
35	chr11:45903600-45906400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr11:45903600-45906600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:45903800-45906400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:45903800-45906400	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr11:45903800-45906600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr11:45903800-45906800	Weak transcription	Aorta	Aorta
41	chr11:45903800-45906800	Weak transcription	Colonic Mucosa	Colon
42	chr11:45903800-45906800	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr11:45903800-45906800	Weak transcription	K562	blood
44	chr11:45904000-45906600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:45904000-45906600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr11:45904000-45906600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr11:45904000-45906600	Weak transcription	Fetal Kidney	kidney
48	chr11:45904000-45906600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr11:45904000-45906600	Weak transcription	Dnd41	blood
50	chr11:45904000-45906600	Weak transcription	HSMMtube	muscle

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