Variant report

Variant	nsv897027
Chromosome Location	chr11:18435700-18499416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:917)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18479092-18479320	HepG2	liver:	n/a	n/a
2	BACH1	chr11:18477287-18477564	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:18441872-18441909	K562	blood:	n/a	n/a
4	BATF	chr11:18490570-18490770	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
5	BATF	chr11:18490527-18490838	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
6	BHLHE40	chr11:18479101-18479289	A549	lung:	n/a	n/a
7	BHLHE40	chr11:18479063-18479387	K562	blood:	n/a	n/a
8	BHLHE40	chr11:18479046-18479396	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:18474554-18474624	K562	blood:	n/a	n/a
10	BRCA1	chr11:18478869-18479367	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:18495203-18495432	HepG2	liver:	n/a	chr11:18495281-18495292
12	CEBPB	chr11:18478449-18479397	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:18491531-18491555	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:18460412-18460437	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:18478565-18478628	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:18495208-18495388	Hela-S3	cervix:	n/a	chr11:18495281-18495292
17	CEBPB	chr11:18452469-18452615	HepG2	liver:	n/a	chr11:18452577-18452588
18	CEBPB	chr11:18444466-18444486	A549	lung:	n/a	n/a
19	CEBPB	chr11:18495235-18495455	K562	blood:	n/a	chr11:18495281-18495292
20	CEBPB	chr11:18495103-18495392	IMR90	lung:	n/a	chr11:18495281-18495292
21	CEBPB	chr11:18488098-18488202	K562	blood:	n/a	n/a
22	CEBPB	chr11:18444389-18444575	K562	blood:	n/a	n/a
23	CEBPB	chr11:18491451-18491642	K562	blood:	n/a	n/a
24	CEBPB	chr11:18488096-18488199	A549	lung:	n/a	n/a
25	CHD2	chr11:18478989-18479353	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr11:18496940-18497090	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr11:18478519-18478550	LNCaP	prostate:	n/a	n/a
28	CTCF	chr11:18478499-18478521	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:18477620-18477770	BE2_C	brain:	n/a	n/a
30	CTCF	chr11:18454783-18454868	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr11:18477602-18477603	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:18477640-18477790	BE2_C	brain:	n/a	n/a
33	CTCF	chr11:18440600-18440750	HepG2	liver:	n/a	n/a
34	CTCF	chr11:18478389-18478505	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:18479840-18479990	GM12867	blood:	n/a	n/a
36	CTCF	chr11:18472348-18472400	GM13976	blood:	n/a	n/a
37	CTCF	chr11:18478556-18478561	LNCaP	prostate:	n/a	n/a
38	CTCF	chr11:18454740-18454890	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr11:18455481-18455501	LNCaP	prostate:	n/a	n/a
40	CTCF	chr11:18484740-18484890	A549	lung:	n/a	n/a
41	CTCF	chr11:18462999-18463059	GM10266	blood:	n/a	n/a
42	CTCF	chr11:18477426-18477601	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:18477719-18477775	GM19239	blood:	n/a	n/a
44	CUX1	chr11:18479381-18479403	K562	blood:	n/a	n/a
45	E2F6	chr11:18477195-18477473	K562	blood:	n/a	chr11:18477378-18477387 chr11:18477355-18477364
46	E2F6	chr11:18477189-18477858	H1-hESC	embryonic stem cell:	n/a	chr11:18477675-18477685 chr11:18477378-18477387 chr11:18477355-18477364
47	E2F6	chr11:18477107-18477718	H1-hESC	embryonic stem cell:	n/a	chr11:18477675-18477685 chr11:18477378-18477387 chr11:18477355-18477364
48	E2F6	chr11:18477224-18477410	K562	blood:	n/a	chr11:18477378-18477387 chr11:18477355-18477364
49	EGR1	chr11:18477231-18477474	K562	blood:	n/a	chr11:18477350-18477363 chr11:18477353-18477363 chr11:18477352-18477362 chr11:18477337-18477352 chr11:18477353-18477362 chr11:18477350-18477364 chr11:18477378-18477387 chr11:18477337-18477347 chr11:18477351-18477362 chr11:18477355-18477365 chr11:18477350-18477363 chr11:18477350-18477363 chr11:18477350-18477363
50	EGR1	chr11:18477110-18477519	K562	blood:	n/a	chr11:18477350-18477363 chr11:18477353-18477363 chr11:18477352-18477362 chr11:18477337-18477352 chr11:18477353-18477362 chr11:18477350-18477364 chr11:18477378-18477387 chr11:18477337-18477347 chr11:18477351-18477362 chr11:18477355-18477365 chr11:18477350-18477363 chr11:18477350-18477363 chr11:18477350-18477363

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18478135-18478185	GM12891	blood:	n/a
2	chr11:18477303-18477353	SKMC	muscle:	n/a
3	chr11:18478135-18478185	GM12891	blood:	n/a
4	chr11:18477303-18477353	SKMC	muscle:	n/a
5	chr11:18477254-18477304	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:18477379-18477429	HCT-116	colon:	n/a
7	chr11:18473775-18473825	ProgFib	skin:	n/a
8	chr11:18476131-18476181	NHBE	bronchial:	n/a
9	chr11:18476131-18476181	MCF-7	breast:	n/a
10	chr11:18481032-18481082	HRCEpiC	kidney:	n/a
11	chr11:18477753-18477803	HEEpiC	esophagus:	n/a
12	chr11:18477153-18477203	HCT-116	colon:	n/a
13	chr11:18478135-18478185	GM12878	blood:	n/a
14	chr11:18481032-18481082	BJ	skin:	n/a
15	chr11:18477299-18477349	HMEC	breast:	n/a
16	chr11:18476081-18476131	AG04450	lung:	fetal
17	chr11:18483771-18483821	HEEpiC	esophagus:	n/a
18	chr11:18477534-18477584	IMR90	lung:	fetal
19	chr11:18477153-18477203	ECC-1	luminal epithelium:	n/a
20	chr11:18476081-18476131	BE2_C	brain:	n/a
21	chr11:18477534-18477584	SK-N-SH	brain:	n/a
22	chr11:18478135-18478185	NHBE	bronchial:	n/a
23	chr11:18477299-18477349	HRE	kidney:	n/a
24	chr11:18477753-18477803	HCF	heart:	n/a
25	chr11:18476131-18476181	HCPEpiC	choroid plexus:	n/a
26	chr11:18477280-18477330	HepG2	liver:	n/a
27	chr11:18476131-18476181	U87	brain:	n/a
28	chr11:18476131-18476181	HRE	kidney:	n/a
29	chr11:18477379-18477429	NT2-D1	testis:	n/a
30	chr11:18477254-18477304	IMR90	lung:	fetal
31	chr11:18478135-18478185	HEEpiC	esophagus:	n/a
32	chr11:18481032-18481082	ProgFib	skin:	n/a
33	chr11:18483771-18483821	NT2-D1	testis:	n/a
34	chr11:18473775-18473825	PANC-1	pancreas:	n/a
35	chr11:18473775-18473825	SK-N-SH	brain:	n/a
36	chr11:18477280-18477330	GM06990	blood:	n/a
37	chr11:18476131-18476181	T-47D	breast:	n/a
38	chr11:18477680-18477730	HIPEpiC	eye:	n/a
39	chr11:18473775-18473825	T-47D	breast:	n/a
40	chr11:18477534-18477584	HMEC	breast:	n/a
41	chr11:18476131-18476181	HNPCEpiC	eye:	n/a
42	chr11:18476131-18476181	CMK	blood:	n/a
43	chr11:18477534-18477584	AG10803	skin:	n/a
44	chr11:18477753-18477803	CMK	blood:	n/a
45	chr11:18473775-18473825	NHDF-neo	bronchial:	n/a
46	chr11:18477680-18477730	HepG2	liver:	n/a
47	chr11:18477303-18477353	AG04449	skin:	fetal
48	chr11:18477280-18477330	PFSK-1	brain:	n/a
49	chr11:18477534-18477584	LNCaP	prostate:	n/a
50	chr11:18477680-18477730	GM06990	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18442100..18443660-chr11:18447182..18449184,2	MCF-7	breast:
2	chr11:18414619..18417567-chr11:18475840..18478644,2	K562	blood:
3	chr11:18456372..18458873-chr11:18461973..18463683,2	K562	blood:
4	chr11:18414985..18417480-chr11:18436029..18437614,2	K562	blood:
5	chr11:18429708..18432011-chr11:18438993..18440849,2	MCF-7	breast:
6	chr11:18415628..18417423-chr11:18491063..18493599,2	MCF-7	breast:
7	chr11:18464968..18467411-chr11:18470062..18474152,3	K562	blood:
8	chr11:18479966..18482806-chr11:18549124..18551467,2	K562	blood:
9	chr11:18474174..18475881-chr11:18477733..18480422,2	MCF-7	breast:
10	chr11:18470144..18471841-chr11:18477720..18480127,2	MCF-7	breast:
11	chr11:18470144..18471841-chr11:18477720..18480127,2	MCF-7	breast:
12	chr11:18442100..18443660-chr11:18447182..18449184,2	MCF-7	breast:
13	chr11:18432049..18434102-chr11:18434419..18436036,2	K562	blood:
14	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
15	chr11:18433811..18435344-chr11:18439087..18441090,2	K562	blood:
16	chr11:18474174..18475881-chr11:18477733..18480422,2	MCF-7	breast:
17	chr11:18464968..18467382-chr11:18471264..18474152,2	K562	blood:
18	chr11:18429091..18432597-chr11:18437736..18442022,5	K562	blood:
19	chr11:18430457..18432481-chr11:18456231..18458824,2	K562	blood:
20	chr11:18429496..18431588-chr11:18458511..18461417,2	K562	blood:
21	chr11:18415718..18417839-chr11:18444013..18446628,2	K562	blood:
22	chr11:18456372..18458873-chr11:18461973..18463683,2	K562	blood:
23	chr11:18415520..18417740-chr11:18457174..18459027,2	K562	blood:
24	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:
25	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
26	chr11:18462496..18464309-chr11:18472211..18474246,2	MCF-7	breast:
27	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSG101-2	chr11:18471659-18472415	NONHSAT018286

No data

Variant related genes	Relation type
LDHAL6A	TF binding region
ENSG00000256734	TF binding region
LDHAL6A	CpG island
ENSG00000256734	CpG island
ENSG00000256734	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000166796	chromatin interactions

Extended variants
information (count: 2165 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2165 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10832934	chr11:18435700-18435701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568503258	chr11:18435735-18435736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535844398	chr11:18435736-18435737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113066977	chr11:18435744-18435745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117263641	chr11:18435817-18435818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373800566	chr11:18435889-18435890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368845044	chr11:18435945-18435946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539257574	chr11:18435981-18435982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557905820	chr11:18436025-18436026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs75762326	chr11:18436028-18436029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543733562	chr11:18436035-18436036	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561625749	chr11:18436081-18436082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112667328	chr11:18436096-18436097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141187582	chr11:18436100-18436101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183428965	chr11:18436117-18436118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187969196	chr11:18436145-18436146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs533000960	chr11:18436200-18436201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552521241	chr11:18436201-18436202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11024648	chr11:18436204-18436205	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs550539770	chr11:18436208-18436209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs137886935	chr11:18436232-18436233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149468315	chr11:18436260-18436261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374780731	chr11:18436264-18436265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547764282	chr11:18436268-18436269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113822754	chr11:18436295-18436296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
26	rs112883073	chr11:18436322-18436323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561502168	chr11:18436332-18436333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144140402	chr11:18436352-18436353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569859426	chr11:18436353-18436354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112382681	chr11:18436373-18436374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536851155	chr11:18436424-18436425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191248232	chr11:18436445-18436446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75305886	chr11:18436448-18436449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
34	rs540628689	chr11:18436470-18436471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139150798	chr11:18436474-18436475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552526077	chr11:18436568-18436569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139946387	chr11:18436578-18436579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368062664	chr11:18436622-18436623	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373305670	chr11:18436680-18436681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370080971	chr11:18436682-18436683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563217843	chr11:18436736-18436737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11558332	chr11:18436759-18436760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376543708	chr11:18436767-18436768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370079739	chr11:18436790-18436791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs551119181	chr11:18436794-18436795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146233108	chr11:18436799-18436800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs151274027	chr11:18436805-18436806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373834035	chr11:18436828-18436829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs367772851	chr11:18436858-18436859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368451212	chr11:18436888-18436889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18430200-18440200	Weak transcription	K562	blood
2	chr11:18434200-18442200	Weak transcription	Pancreas	Pancrea
3	chr11:18434400-18438800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:18435000-18436000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:18436000-18442000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:18440200-18441800	Enhancers	K562	blood
7	chr11:18441800-18442400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:18442000-18442400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr11:18442000-18442600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr11:18442000-18442600	Enhancers	HUVEC	blood vessel
11	chr11:18442000-18442800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:18442000-18442800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:18450800-18451200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:18451000-18451400	Enhancers	K562	blood
15	chr11:18457200-18479200	Weak transcription	Pancreas	Pancrea
16	chr11:18463200-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:18463400-18463800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:18463400-18464000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr11:18471000-18471400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr11:18474200-18475000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:18474400-18474800	Enhancers	NHDF-Ad	bronchial
24	chr11:18474400-18475000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:18474400-18475000	Enhancers	Hela-S3	cervix
26	chr11:18475000-18476000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:18476000-18476200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:18476800-18477000	Active TSS	Spleen	Spleen
29	chr11:18477000-18477200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:18477000-18477600	Enhancers	Spleen	Spleen
31	chr11:18477200-18477400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:18477200-18477400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:18477200-18477600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:18477200-18477800	Active TSS	Brain Germinal Matrix	brain
35	chr11:18477200-18477800	Active TSS	Ovary	ovary
36	chr11:18477200-18478000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:18477400-18477600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
38	chr11:18477400-18477600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr11:18477400-18477600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:18477400-18477600	Bivalent Enhancer	Right Ventricle	heart
41	chr11:18477400-18477800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:18477400-18477800	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr11:18477400-18477800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr11:18477400-18477800	Active TSS	Fetal Brain Female	brain
45	chr11:18477400-18478000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:18477400-18478000	Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr11:18477400-18478000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
48	chr11:18477600-18477800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:18477600-18477800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:18477600-18478200	Enhancers	Right Ventricle	heart

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