Variant report

Variant	nsv897010
Chromosome Location	chr11:15219258-15279421
allele	n/a
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	ARID3A	chr11:15235422-15235795	HepG2	liver:	n/a	n/a
2	ATF1	chr11:15269085-15269109	K562	blood:	n/a	n/a
3	BHLHE40	chr11:15230205-15230498	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:15230233-15230409	K562	blood:	n/a	n/a
5	BRCA1	chr11:15230212-15230410	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:15234438-15234765	HepG2	liver:	n/a	chr11:15234606-15234615 chr11:15234604-15234615 chr11:15234605-15234616
7	CEBPB	chr11:15228226-15228541	A549	lung:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
8	CEBPB	chr11:15228262-15228602	Hela-S3	cervix:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
9	CEBPB	chr11:15228183-15228554	IMR90	lung:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
10	CEBPB	chr11:15228208-15228656	HepG2	liver:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
11	CEBPB	chr11:15234481-15234745	K562	blood:	n/a	chr11:15234606-15234615 chr11:15234604-15234615 chr11:15234605-15234616
12	CEBPB	chr11:15242125-15242398	IMR90	lung:	n/a	n/a
13	CEBPB	chr11:15273687-15273997	K562	blood:	n/a	n/a
14	CEBPB	chr11:15228218-15228526	K562	blood:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
15	CEBPB	chr11:15242079-15242343	A549	lung:	n/a	n/a
16	CEBPB	chr11:15230212-15230502	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:15273707-15273946	A549	lung:	n/a	n/a
18	CHD1	chr11:15221208-15221212	GM12878	blood:	n/a	n/a
19	CHD2	chr11:15230171-15230458	H1-hESC	embryonic stem cell:	n/a	chr11:15230210-15230217
20	CHD2	chr11:15222723-15222896	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr11:15238320-15238470	GM12874	blood:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
22	CTCF	chr11:15229880-15230030	NHLF	lung:	n/a	n/a
23	CTCF	chr11:15230260-15230410	NB4	blood:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
24	CTCF	chr11:15238345-15238553	HUVEC	blood vessel:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
25	CTCF	chr11:15238360-15238510	SK-N-SH_RA	brain:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
26	CTCF	chr11:15238360-15238510	HPAF	blood vessel:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
27	CTCF	chr11:15238340-15238490	HFF-Myc	foreskin:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
28	CTCF	chr11:15230300-15230450	HCPEpiC	choroid plexus:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
29	CTCF	chr11:15230440-15230590	A549	lung:	n/a	n/a
30	CTCF	chr11:15230680-15230830	GM12873	blood:	n/a	n/a
31	CTCF	chr11:15230280-15230430	HCFaa	heart:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
32	CTCF	chr11:15238360-15238510	HPF	lung:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
33	CTCF	chr11:15238380-15238530	GM12865	blood:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
34	CTCF	chr11:15238340-15238490	GM12872	blood:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
35	CTCF	chr11:15230200-15230519	MCF-7	breast:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
36	CTCF	chr11:15238660-15238810	AG04450	lung:	n/a	n/a
37	CTCF	chr11:15219520-15219670	AG09309	skin:	n/a	n/a
38	CTCF	chr11:15219840-15219990	AG10803	skin:	n/a	chr11:15219884-15219902
39	CTCF	chr11:15230280-15230430	HRE	kidney:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
40	CTCF	chr11:15237940-15238090	A549	lung:	n/a	n/a
41	CTCF	chr11:15238309-15238544	GM12891	blood:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
42	CTCF	chr11:15238400-15238550	AG04450	lung:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
43	CTCF	chr11:15219840-15219990	NHLF	lung:	n/a	chr11:15219884-15219902
44	CTCF	chr11:15238380-15238530	NHDF-neo	bronchial:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
45	CTCF	chr11:15230613-15230756	GM10266	blood:	n/a	n/a
46	CTCF	chr11:15230280-15230430	AoAF	blood vessel:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
47	CTCF	chr11:15238320-15238470	HFF-Myc	foreskin:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
48	CTCF	chr11:15230340-15230490	HMEC	breast:	n/a	chr11:15230352-15230362 chr11:15230355-15230364 chr11:15230349-15230367 chr11:15230350-15230366 chr11:15230344-15230365
49	CTCF	chr11:15238330-15238573	K562	blood:	n/a	chr11:15238409-15238418 chr11:15238406-15238419
50	CTCF	chr11:15246260-15246410	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15220058-15220108	AoSMC	blood vessel:	n/a
2	chr11:15229502-15229552	HIPEpiC	eye:	n/a
3	chr11:15220058-15220108	HepG2	liver:	n/a
4	chr11:15268469-15268519	HepG2	liver:	n/a
5	chr11:15268469-15268519	NB4	blood:	n/a
6	chr11:15220058-15220108	HL-60	blood:	n/a
7	chr11:15268469-15268519	PANC-1	pancreas:	n/a
8	chr11:15268469-15268519	HIPEpiC	eye:	n/a
9	chr11:15268469-15268519	HRE	kidney:	n/a
10	chr11:15220058-15220108	Caco-2	colon:	n/a
11	chr11:15258312-15258362	HEK293	kidney:	embryo
12	chr11:15230314-15230364	AG09319	gingival:	n/a
13	chr11:15230314-15230364	GM19239	blood:	n/a
14	chr11:15268469-15268519	Hepatocyte	liver:	n/a
15	chr11:15220058-15220108	GM06990	blood:	n/a
16	chr11:15268469-15268519	GM19239	blood:	n/a
17	chr11:15229502-15229552	AG04450	lung:	fetal
18	chr11:15268469-15268519	SKMC	muscle:	n/a
19	chr11:15220058-15220108	BE2_C	brain:	n/a
20	chr11:15268469-15268519	SK-N-MC	brain:	n/a
21	chr11:15230314-15230364	HAEpiC	amniotic membrane:	n/a
22	chr11:15268469-15268519	K562	blood:	n/a
23	chr11:15268469-15268519	NHDF-neo	bronchial:	n/a
24	chr11:15229502-15229552	NHBE	bronchial:	n/a
25	chr11:15258312-15258362	IMR90	lung:	fetal
26	chr11:15229502-15229552	GM06990	blood:	n/a
27	chr11:15229502-15229552	GM12878	blood:	n/a
28	chr11:15268469-15268519	HMEC	breast:	n/a
29	chr11:15230314-15230364	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:15230314-15230364	SK-N-SH	brain:	n/a
31	chr11:15268469-15268519	NHBE	bronchial:	n/a
32	chr11:15268469-15268519	HUVEC	blood vessel:	n/a
33	chr11:15220058-15220108	SKMC	muscle:	n/a
34	chr11:15230314-15230364	SK-N-SH_RA	brain:	n/a
35	chr11:15230314-15230364	K562	blood:	n/a
36	chr11:15268469-15268519	HEEpiC	esophagus:	n/a
37	chr11:15230314-15230364	H1-hESC	embryonic stem cell:	embryo
38	chr11:15220058-15220108	MCF10A-Er-Src	breast:	n/a
39	chr11:15229502-15229552	PANC-1	pancreas:	n/a
40	chr11:15229502-15229552	RPTEC	kidney:	n/a
41	chr11:15220058-15220108	AG10803	skin:	n/a
42	chr11:15230314-15230364	HCPEpiC	choroid plexus:	n/a
43	chr11:15230314-15230364	HCM	heart:	n/a
44	chr11:15230314-15230364	Caco-2	colon:	n/a
45	chr11:15220058-15220108	PANC-1	pancreas:	n/a
46	chr11:15220058-15220108	HUVEC	blood vessel:	n/a
47	chr11:15258312-15258362	NHDF-neo	bronchial:	n/a
48	chr11:15258312-15258362	HCM	heart:	n/a
49	chr11:15268469-15268519	AG09309	skin:	n/a
50	chr11:15258312-15258362	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:15222139..15224129-chr11:15224324..15225879,2	K562	blood:
2	chr11:15122385..15123116-chr11:15238390..15238956,3	K562	blood:
3	chr11:15222139..15224129-chr11:15224324..15225879,2	K562	blood:
4	chr11:14929842..14930739-chr11:15229981..15230831,5	K562	blood:
5	chr11:14929858..14930710-chr11:15230022..15230796,4	MCF-7	breast:
6	chr11:15094886..15096748-chr11:15229663..15231358,2	MCF-7	breast:
7	chr11:15214458..15216494-chr11:15217600..15220011,2	K562	blood:
8	chr11:15060394..15061162-chr11:15238309..15238839,2	MCF-7	breast:
9	chr11:15122346..15123401-chr11:15229849..15230871,9	K562	blood:
10	chr11:15121462..15122175-chr11:15230252..15230842,2	MCF-7	breast:
11	chr11:15238033..15238920-chr11:15246673..15247245,2	MCF-7	breast:
12	chr11:15230302..15230837-chr11:15238045..15239014,2	MCF-7	breast:
13	chr11:15265846..15267612-chr11:15271655..15273612,2	K562	blood:
14	chr11:15262063..15264369-chr11:15524628..15526995,2	K562	blood:
15	chr11:15238033..15238920-chr11:15246673..15247245,2	MCF-7	breast:
16	chr11:15122345..15123510-chr11:15229905..15230828,9	MCF-7	breast:
17	chr11:15122329..15123323-chr11:15229850..15230841,5	MCF-7	breast:
18	chr11:15236431..15237945-chr11:15241172..15243025,2	MCF-7	breast:
19	chr11:15236431..15237945-chr11:15241172..15243025,2	MCF-7	breast:
20	chr11:15265846..15267612-chr11:15271655..15273612,2	K562	blood:
21	chr11:15230303..15231896-chr11:15234367..15236672,2	K562	blood:
22	chr11:15230303..15231896-chr11:15234367..15236672,2	K562	blood:
23	chr11:14991233..14992001-chr11:15230234..15230829,2	MCF-7	breast:
24	chr11:15230302..15230837-chr11:15238045..15239014,2	MCF-7	breast:

Variant related genes	Relation type
INSC	TF binding region
INSC	CpG island
ENSG00000110680	chromatin interactions
ENSG00000175868	chromatin interactions

Extended variants
information (count: 2449 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2449 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1945637	chr11:15219258-15219259	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551938288	chr11:15219274-15219275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571046560	chr11:15219313-15219314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148216437	chr11:15219321-15219322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550529145	chr11:15219322-15219323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192911208	chr11:15219325-15219326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184846284	chr11:15219326-15219327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141274737	chr11:15219331-15219332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140714838	chr11:15219344-15219345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528167274	chr11:15219399-15219400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548185737	chr11:15219439-15219440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147404609	chr11:15219462-15219463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138236301	chr11:15219527-15219528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374441938	chr11:15219554-15219555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs66566908	chr11:15219555-15219556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143742015	chr11:15219614-15219615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115361597	chr11:15219618-15219619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372788249	chr11:15219622-15219623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71455854	chr11:15219639-15219640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556082981	chr11:15219650-15219651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569974322	chr11:15219653-15219654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73426533	chr11:15219698-15219699	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374503820	chr11:15219770-15219771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187184043	chr11:15219808-15219809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560093949	chr11:15219919-15219920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191193134	chr11:15219920-15219921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545898376	chr11:15219987-15219988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538850452	chr11:15220004-15220005	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564009415	chr11:15220011-15220012	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183737619	chr11:15220051-15220052	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368450457	chr11:15220058-15220059	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531969008	chr11:15220059-15220060	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75804471	chr11:15220061-15220062	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562410563	chr11:15220064-15220065	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188206928	chr11:15220065-15220066	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1540151	chr11:15220073-15220074	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs566090621	chr11:15220082-15220083	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367992225	chr11:15220120-15220121	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534791419	chr11:15220212-15220213	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71455855	chr11:15220270-15220271	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539419337	chr11:15220294-15220295	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139698584	chr11:15220311-15220312	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1540152	chr11:15220404-15220405	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs369421728	chr11:15220491-15220492	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149345769	chr11:15220492-15220493	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11023470	chr11:15220540-15220541	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531642734	chr11:15220564-15220565	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116323402	chr11:15220603-15220604	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553748726	chr11:15220630-15220631	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115620361	chr11:15220682-15220683	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Myelofibrosis	22110671	CNVD
Cancer	24489367	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15197800-15221000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:15210000-15220600	Weak transcription	Aorta	Aorta
3	chr11:15212200-15220800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:15215800-15222000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:15215800-15222000	Enhancers	NHDF-Ad	bronchial
6	chr11:15215800-15222000	Enhancers	Osteobl	bone
7	chr11:15216200-15222200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr11:15216600-15219600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr11:15216600-15222000	Enhancers	Colon Smooth Muscle	Colon
10	chr11:15217200-15219800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:15217200-15222600	Enhancers	Liver	Liver
12	chr11:15217400-15219600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr11:15217400-15219800	Weak transcription	NH-A	brain
14	chr11:15217400-15220800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:15217800-15219600	Weak transcription	Fetal Muscle Leg	muscle
16	chr11:15218000-15219400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:15218000-15219600	Weak transcription	HSMMtube	muscle
18	chr11:15218000-15220000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr11:15218000-15222000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:15218200-15219400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr11:15218600-15221200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:15218600-15229400	Weak transcription	Gastric	stomach
23	chr11:15218800-15219400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:15218800-15220200	Enhancers	Fetal Stomach	stomach
25	chr11:15218800-15222600	Enhancers	Fetal Brain Male	brain
26	chr11:15219000-15220000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:15219000-15220000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:15219000-15220600	Enhancers	Fetal Lung	lung
29	chr11:15219200-15221000	Weak transcription	Pancreas	Pancrea
30	chr11:15219200-15221800	Enhancers	Stomach Smooth Muscle	stomach
31	chr11:15219200-15234600	Weak transcription	Fetal Intestine Small	intestine
32	chr11:15219400-15219800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr11:15219400-15220800	Enhancers	Fetal Brain Female	brain
34	chr11:15219400-15223000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr11:15219400-15223200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:15219600-15219800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr11:15219600-15220000	Enhancers	Brain Germinal Matrix	brain
38	chr11:15219600-15220000	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr11:15219600-15220000	Enhancers	HSMMtube	muscle
40	chr11:15219600-15220200	Enhancers	Fetal Muscle Leg	muscle
41	chr11:15219600-15221400	Enhancers	Rectal Smooth Muscle	rectum
42	chr11:15219800-15220000	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr11:15219800-15220000	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr11:15219800-15220000	Enhancers	NH-A	brain
45	chr11:15219800-15222400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:15220000-15221000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:15220000-15221000	Weak transcription	Brain Germinal Matrix	brain
48	chr11:15220000-15221200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:15220000-15221200	Weak transcription	HSMMtube	muscle
50	chr11:15220000-15221800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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