Variant report

Variant	esv1836937
Chromosome Location	chr11:17291499-17339127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:788)
CpG islands
(count:793)
Chromatin interactive
region (count:42)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17297923-17298398	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17298969-17299169	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:17297898-17298099	K562	blood:	n/a	n/a
4	ARID3A	chr11:17296980-17297198	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:17298792-17299541	K562	blood:	n/a	n/a
6	ATF2	chr11:17319713-17320319	GM12878	blood:	n/a	n/a
7	ATF2	chr11:17315495-17315916	GM12878	blood:	n/a	n/a
8	ATF2	chr11:17315464-17316124	GM12878	blood:	n/a	n/a
9	ATF2	chr11:17297511-17298222	GM12878	blood:	n/a	n/a
10	ATF2	chr11:17319739-17320323	GM12878	blood:	n/a	n/a
11	BACH1	chr11:17298260-17298283	K562	blood:	n/a	n/a
12	BACH1	chr11:17297732-17298136	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:17319816-17320200	GM12878	blood:	n/a	n/a
14	BATF	chr11:17318368-17318670	GM12878	blood:	n/a	n/a
15	BATF	chr11:17318396-17318651	GM12878	blood:	n/a	n/a
16	BATF	chr11:17315531-17315975	GM12878	blood:	n/a	n/a
17	BATF	chr11:17319777-17320285	GM12878	blood:	n/a	n/a
18	BATF	chr11:17315562-17315887	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:17319838-17320210	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:17297676-17297972	GM12878	blood:	n/a	chr11:17297921-17297934
21	BCL11A	chr11:17319811-17320210	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:17315561-17315939	GM12878	blood:	n/a	n/a
23	BCL3	chr11:17319744-17320237	GM12878	blood:	n/a	n/a
24	BCL3	chr11:17319803-17320138	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:17297494-17298127	GM12878	blood:	n/a	chr11:17297921-17297934
26	BCLAF1	chr11:17319783-17320311	GM12878	blood:	n/a	n/a
27	BCLAF1	chr11:17297565-17298269	GM12878	blood:	n/a	chr11:17297921-17297934
28	BCLAF1	chr11:17319803-17320210	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:17295385-17295781	K562	blood:	n/a	n/a
30	BHLHE40	chr11:17296990-17297125	K562	blood:	n/a	n/a
31	BHLHE40	chr11:17336006-17336007	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:17297695-17298420	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:17299200-17299254	K562	blood:	n/a	n/a
34	BHLHE40	chr11:17295569-17295756	HepG2	liver:	n/a	n/a
35	BHLHE40	chr11:17307409-17307597	K562	blood:	n/a	n/a
36	BHLHE40	chr11:17297760-17298982	K562	blood:	n/a	n/a
37	BHLHE40	chr11:17319916-17320153	GM12878	blood:	n/a	n/a
38	BRCA1	chr11:17297802-17298362	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr11:17297916-17298248	HepG2	liver:	n/a	n/a
40	BRCA1	chr11:17298218-17298315	GM12878	blood:	n/a	n/a
41	CBX3	chr11:17297562-17299170	K562	blood:	n/a	n/a
42	CBX3	chr11:17297691-17298085	K562	blood:	n/a	n/a
43	CCNT2	chr11:17297699-17298813	K562	blood:	n/a	chr11:17298432-17298452 chr11:17298425-17298434
44	CEBPB	chr11:17297848-17298307	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:17304269-17304472	HepG2	liver:	n/a	chr11:17304409-17304420
46	CEBPB	chr11:17313606-17313609	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:17319896-17320187	GM12878	blood:	n/a	n/a
48	CEBPB	chr11:17302088-17302280	A549	lung:	n/a	chr11:17302231-17302242
49	CEBPB	chr11:17296631-17297246	K562	blood:	n/a	chr11:17297043-17297054
50	CEBPB	chr11:17298800-17299118	Hela-S3	cervix:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17300909-17300959	Caco-2	colon:	n/a
2	chr11:17298266-17298316	Jurkat	blood:	n/a
3	chr11:17298264-17298314	HRCEpiC	kidney:	n/a
4	chr11:17298537-17298587	Caco-2	colon:	n/a
5	chr11:17294197-17294247	Jurkat	blood:	n/a
6	chr11:17297732-17297782	HCT-116	colon:	n/a
7	chr11:17298048-17298098	ProgFib	skin:	n/a
8	chr11:17298264-17298314	HCPEpiC	choroid plexus:	n/a
9	chr11:17298266-17298316	PrEC	prostate:	n/a
10	chr11:17298537-17298587	CMK	blood:	n/a
11	chr11:17298268-17298318	AG09309	skin:	n/a
12	chr11:17298537-17298587	MCF-7	breast:	n/a
13	chr11:17294197-17294247	NHBE	bronchial:	n/a
14	chr11:17294197-17294247	HCM	heart:	n/a
15	chr11:17298266-17298316	ovcar-3	ovarian:	n/a
16	chr11:17298266-17298316	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:17298264-17298314	BE2_C	brain:	n/a
18	chr11:17300909-17300959	NB4	blood:	n/a
19	chr11:17298266-17298316	NT2-D1	testis:	n/a
20	chr11:17298347-17298397	GM19239	blood:	n/a
21	chr11:17298260-17298310	Hela-S3	cervix:	n/a
22	chr11:17298260-17298310	NHDF-neo	bronchial:	n/a
23	chr11:17298260-17298310	HRPEpiC	eye:	n/a
24	chr11:17297984-17298034	RPTEC	kidney:	n/a
25	chr11:17300909-17300959	GM06990	blood:	n/a
26	chr11:17297732-17297782	HCPEpiC	choroid plexus:	n/a
27	chr11:17298537-17298587	LNCaP	prostate:	n/a
28	chr11:17298273-17298323	GM19239	blood:	n/a
29	chr11:17298266-17298316	HRCEpiC	kidney:	n/a
30	chr11:17297732-17297782	MCF10A-Er-Src	breast:	n/a
31	chr11:17298273-17298323	MCF-7	breast:	n/a
32	chr11:17298537-17298587	AG09309	skin:	n/a
33	chr11:17298268-17298318	ovcar-3	ovarian:	n/a
34	chr11:17300909-17300959	GM12891	blood:	n/a
35	chr11:17298064-17298114	HAEpiC	amniotic membrane:	n/a
36	chr11:17298268-17298318	ECC-1	luminal epithelium:	n/a
37	chr11:17300909-17300959	T-47D	breast:	n/a
38	chr11:17298064-17298114	AG10803	skin:	n/a
39	chr11:17298537-17298587	HUVEC	blood vessel:	n/a
40	chr11:17297732-17297782	HAEpiC	amniotic membrane:	n/a
41	chr11:17297732-17297782	SAEC	small airway:	n/a
42	chr11:17298537-17298587	GM12878	blood:	n/a
43	chr11:17297732-17297782	K562	blood:	n/a
44	chr11:17298048-17298098	GM12891	blood:	n/a
45	chr11:17298266-17298316	HMEC	breast:	n/a
46	chr11:17298064-17298114	HRPEpiC	eye:	n/a
47	chr11:17297984-17298034	NHBE	bronchial:	n/a
48	chr11:17298273-17298323	AoSMC	blood vessel:	n/a
49	chr11:17298268-17298318	HRCEpiC	kidney:	n/a
50	chr11:17298064-17298114	NB4	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17297226..17298077-chr5:43007702..43008379,2	NB4	blood:
2	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
3	chr11:17260848..17261373-chr11:17294457..17295035,2	MCF-7	breast:
4	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
5	chr11:17293894..17295404-chr11:17299540..17302043,2	K562	blood:
6	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
7	chr11:17324227..17326282-chr11:17370624..17372568,2	K562	blood:
8	chr11:17293894..17295404-chr11:17299540..17302043,2	K562	blood:
9	chr11:17312629..17314667-chr11:17373506..17375869,2	K562	blood:
10	chr11:17325618..17327534-chr11:17329034..17330695,2	K562	blood:
11	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
12	chr11:17260848..17261450-chr11:17294076..17295035,3	MCF-7	breast:
13	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
14	chr1:236030459..236030960-chr11:17297574..17298074,2	Hela-S3	cervix:
15	chr11:17297507..17298318-chr9:140135332..140136049,2	NB4	blood:
16	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
17	chr11:17336064..17337683-chr11:17338247..17340454,2	MCF-7	breast:
18	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
19	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
20	chr11:17279766..17282636-chr11:17296129..17298031,2	MCF-7	breast:
21	chr11:17296907..17298912-chr11:17352213..17353767,2	K562	blood:
22	chr11:17296529..17299421-chr11:17301500..17303584,3	K562	blood:
23	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:
24	chr11:17336111..17336712-chr4:31786899..31787441,2	MCF-7	breast:
25	chr11:17097827..17101102-chr11:17296839..17299555,4	K562	blood:
26	chr11:17286631..17289597-chr11:17295588..17297647,2	MCF-7	breast:
27	chr11:17290835..17293391-chr11:17295443..17297735,3	K562	blood:
28	chr11:17325618..17327534-chr11:17329034..17330695,2	K562	blood:
29	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:
30	chr11:17289797..17291811-chr11:17310885..17313618,2	MCF-7	breast:
31	chr11:17336064..17337683-chr11:17338247..17340454,2	MCF-7	breast:
32	chr11:17289393..17293255-chr11:17296129..17299283,5	K562	blood:
33	chr11:17290835..17293391-chr11:17295443..17297735,3	K562	blood:
34	chr11:17297839..17299498-chr11:17314289..17315941,2	K562	blood:
35	chr11:17289393..17293255-chr11:17296129..17299283,5	K562	blood:
36	chr11:17326206..17329035-chr11:17373142..17375618,2	K562	blood:
37	chr11:17297568..17298688-chr6:26123742..26124744,3	Hela-S3	cervix:
38	chr11:17294885..17299963-chr11:17371989..17377835,11	K562	blood:
39	chr11:17229045..17230754-chr11:17298034..17300385,2	MCF-7	breast:
40	chr11:14541378..14542196-chr11:17298214..17298716,2	NB4	blood:
41	chr11:17097070..17101102-chr11:17296326..17299484,3	K562	blood:
42	chr11:17229425..17232064-chr11:17297458..17300131,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNJ11-5	chr11:17327447-17328093	l_439_chr11:17315763-17328093_testes
2	lnc-RP1-239B22.1.1-2	chr11:17304336-17304417	NONHSAT018222
3	lnc-KCNJ11-5	chr11:17315764-17315875	l_439_chr11:17315763-17328093_testes
4	lnc-RP1-239B22.1.1-2	chr11:17299909-17300084	NONHSAT018222
5	lnc-RP1-239B22.1.1-2	chr11:17317652-17317713	NONHSAT018223
6	lnc-RP1-239B22.1.1-2	chr11:17316872-17317014	NONHSAT018223
7	lnc-RP1-239B22.1.1-2	chr11:17298278-17298375	NONHSAT018222
8	lnc-KCNJ11-5	chr11:17328921-17329034	l_439_chr11:17315763-17328093_testes
9	lnc-KCNJ11-5	chr11:17315881-17316560	l_439_chr11:17315763-17328093_testes
10	lnc-RP1-239B22.1.1-2	chr11:17298287-17298395	NONHSAT018223
11	lnc-RP1-239B22.1.1-2	chr11:17304337-17304490	NONHSAT018223
12	lnc-KCNJ11-5	chr11:17329160-17329300	l_439_chr11:17315763-17328093_testes

No data

Variant related genes	Relation type
NUCB2	TF binding region
NUCB2	CpG island
ENSG00000256206	chromatin interactions
ENSG00000129084	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000188211	chromatin interactions

Extended variants
information (count: 1650 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs214097	chr11:17291499-17291500	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377678814	chr11:17291519-17291520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537534183	chr11:17291520-17291521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550047199	chr11:17291521-17291522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs74802941	chr11:17291541-17291542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568395454	chr11:17291580-17291581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535719775	chr11:17291594-17291595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114857663	chr11:17291625-17291626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566102036	chr11:17291628-17291629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188873916	chr11:17291630-17291631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557557637	chr11:17291640-17291641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs117747889	chr11:17291761-17291762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537022478	chr11:17291833-17291834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181322578	chr11:17291855-17291856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372399839	chr11:17291907-17291908	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148179288	chr11:17291908-17291909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143809333	chr11:17291911-17291912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541284602	chr11:17291912-17291913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568164663	chr11:17291950-17291951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374409082	chr11:17291977-17291978	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577760728	chr11:17291979-17291980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150711442	chr11:17292012-17292013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564411281	chr11:17292030-17292031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs105290	chr11:17292068-17292069	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs376176173	chr11:17292084-17292085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549884742	chr11:17292201-17292202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191047639	chr11:17292202-17292203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529260258	chr11:17292220-17292221	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535603973	chr11:17292255-17292256	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79348327	chr11:17292294-17292295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs73417208	chr11:17292302-17292303	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs139047834	chr11:17292306-17292307	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570284165	chr11:17292363-17292364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537106094	chr11:17292411-17292412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149525576	chr11:17292416-17292417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs80137068	chr11:17292466-17292467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs180718489	chr11:17292530-17292531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540177110	chr11:17292540-17292541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573139308	chr11:17292546-17292547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187469170	chr11:17292556-17292557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577905513	chr11:17292566-17292567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540356059	chr11:17292569-17292570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191878985	chr11:17292572-17292573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144144754	chr11:17292584-17292585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183308212	chr11:17292685-17292686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs214096	chr11:17292698-17292699	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187638663	chr11:17292750-17292751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112674260	chr11:17292851-17292852	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561850302	chr11:17292901-17292902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529248240	chr11:17292905-17292906	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
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17286000-17294400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:17286000-17294400	Weak transcription	Hela-S3	cervix
3	chr11:17286000-17297200	Weak transcription	A549	lung
4	chr11:17286000-17297400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:17289200-17294400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:17289200-17295400	Weak transcription	Placenta	Placenta
7	chr11:17289400-17294400	Weak transcription	Thymus	Thymus
8	chr11:17289400-17295400	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr11:17290200-17294200	Weak transcription	NHEK	skin
10	chr11:17290400-17294200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:17290400-17294400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:17290800-17294200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr11:17290800-17294400	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr11:17290800-17294400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr11:17290800-17295400	Weak transcription	K562	blood
16	chr11:17291000-17294000	Weak transcription	Dnd41	blood
17	chr11:17291000-17294400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:17293800-17297200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr11:17294000-17297000	Enhancers	Dnd41	blood
20	chr11:17294200-17295000	Enhancers	NHEK	skin
21	chr11:17294200-17297400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr11:17294200-17297400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr11:17294200-17297600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:17294400-17294600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:17294400-17294600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:17294400-17294600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr11:17294400-17294600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:17294400-17294600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:17294400-17294600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:17294400-17294600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:17294400-17294600	ZNF genes & repeats	Aorta	Aorta
32	chr11:17294400-17294600	Enhancers	Gastric	stomach
33	chr11:17294400-17294600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr11:17294400-17294600	Active TSS	HepG2	liver
35	chr11:17294400-17294600	Enhancers	HMEC	breast
36	chr11:17294400-17294800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:17294400-17294800	Enhancers	Fetal Kidney	kidney
38	chr11:17294400-17294800	Flanking Active TSS	Hela-S3	cervix
39	chr11:17294400-17294800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr11:17294400-17295000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:17294400-17295000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr11:17294400-17295000	Enhancers	Thymus	Thymus
43	chr11:17294400-17295200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:17294400-17295800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:17294400-17295800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:17294400-17295800	Enhancers	Esophagus	oesophagus
47	chr11:17294400-17297400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:17294400-17297400	Enhancers	Fetal Thymus	thymus
49	chr11:17294400-17297600	Enhancers	Primary hematopoietic stem cells	blood
50	chr11:17294600-17294800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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