Variant report

Variant	nsv982925
Chromosome Location	chr11:18132176-18153921
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	chr11:18136953-18137373	HepG2	liver:	n/a	n/a
2	BHLHE40	chr11:18137111-18137377	GM12878	blood:	n/a	n/a
3	BRCA1	chr11:18137153-18137424	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr11:18153079-18153202	HepG2	liver:	n/a	n/a
5	CEBPB	chr11:18152991-18153228	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:18143062-18143194	HepG2	liver:	n/a	chr11:18143125-18143136
7	CEBPB	chr11:18152968-18153327	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:18152988-18153271	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:18152983-18153256	A549	lung:	n/a	n/a
10	CEBPB	chr11:18153050-18153193	K562	blood:	n/a	n/a
11	CEBPB	chr11:18143006-18143270	HepG2	liver:	n/a	chr11:18143125-18143136
12	CEBPB	chr11:18153094-18153283	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr11:18142831-18143084	HepG2	liver:	n/a	n/a
14	CHD2	chr11:18137163-18137434	HepG2	liver:	n/a	n/a
15	CTCF	chr11:18137079-18137427	GM12892	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
16	CTCF	chr11:18137180-18137330	HepG2	liver:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
17	CTCF	chr11:18137160-18137310	HPF	lung:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
18	CTCF	chr11:18137443-18137596	GM12892	blood:	n/a	n/a
19	CTCF	chr11:18137140-18137290	GM12867	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
20	CTCF	chr11:18137140-18137290	HFF-Myc	foreskin:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
21	CTCF	chr11:18137140-18137290	HA-sp	spinal cord:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
22	CTCF	chr11:18137180-18137330	HMF	breast:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
23	CTCF	chr11:18137160-18137310	HRPEpiC	eye:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
24	CTCF	chr11:18137120-18137270	A549	lung:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
25	CTCF	chr11:18137120-18137270	HCT-116	colon:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
26	CTCF	chr11:18136904-18136946	GM12878	blood:	n/a	n/a
27	CTCF	chr11:18137099-18137361	MCF-7	breast:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
28	CTCF	chr11:18137120-18137270	HRE	kidney:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
29	CTCF	chr11:18137106-18137342	GM13977	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
30	CTCF	chr11:18137079-18137400	SK-N-SH_RA	brain:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
31	CTCF	chr11:18137506-18137550	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:18137160-18137310	GM12865	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
33	CTCF	chr11:18137160-18137310	MCF-7	breast:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
34	CTCF	chr11:18137160-18137310	GM12870	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
35	CTCF	chr11:18136840-18136990	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr11:18136768-18137696	SK-N-SH	brain:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
37	CTCF	chr11:18137079-18137375	K562	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
38	CTCF	chr11:18137491-18137568	GM12891	blood:	n/a	n/a
39	CTCF	chr11:18137440-18137590	AG09309	skin:	n/a	n/a
40	CTCF	chr11:18137076-18137424	K562	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
41	CTCF	chr11:18137030-18137452	T-47D	breast:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
42	CTCF	chr11:18137140-18137290	RPTEC	kidney:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
43	CTCF	chr11:18137099-18137362	T-47D	breast:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
44	CTCF	chr11:18137160-18137310	SAEC	small airway:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
45	CTCF	chr11:18137025-18137423	A549	lung:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
46	CTCF	chr11:18137140-18137290	BE2_C	brain:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
47	CTCF	chr11:18137109-18137351	H1-hESC	embryonic stem cell:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
48	CTCF	chr11:18137160-18137310	HVMF	connective:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
49	CTCF	chr11:18137101-18137351	Hela-S3	cervix:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240
50	CTCF	chr11:18137120-18137270	GM12870	blood:	n/a	chr11:18137225-18137234 chr11:18137224-18137245 chr11:18137223-18137239 chr11:18137225-18137238 chr11:18137222-18137240

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18138394-18138444	ProgFib	skin:	n/a
2	chr11:18138837-18138887	BE2_C	brain:	n/a
3	chr11:18139019-18139069	HUVEC	blood vessel:	n/a
4	chr11:18138394-18138444	SK-N-MC	brain:	n/a
5	chr11:18137155-18137205	HMEC	breast:	n/a
6	chr11:18138394-18138444	SKMC	muscle:	n/a
7	chr11:18138394-18138444	GM19239	blood:	n/a
8	chr11:18138837-18138887	GM12878	blood:	n/a
9	chr11:18141393-18141443	GM12891	blood:	n/a
10	chr11:18138837-18138887	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:18141625-18141675	AoSMC	blood vessel:	n/a
12	chr11:18141625-18141675	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:18141625-18141675	HepG2	liver:	n/a
14	chr11:18137155-18137205	HEEpiC	esophagus:	n/a
15	chr11:18139019-18139069	HCPEpiC	choroid plexus:	n/a
16	chr11:18141625-18141675	LNCaP	prostate:	n/a
17	chr11:18138394-18138444	Caco-2	colon:	n/a
18	chr11:18141393-18141443	H1-hESC	embryonic stem cell:	embryo
19	chr11:18138837-18138887	CMK	blood:	n/a
20	chr11:18141625-18141675	Hela-S3	cervix:	n/a
21	chr11:18138394-18138444	BE2_C	brain:	n/a
22	chr11:18138837-18138887	HL-60	blood:	n/a
23	chr11:18138837-18138887	IMR90	lung:	fetal
24	chr11:18138837-18138887	BJ	skin:	n/a
25	chr11:18141625-18141675	MCF-7	breast:	n/a
26	chr11:18139019-18139069	GM06990	blood:	n/a
27	chr11:18141393-18141443	BE2_C	brain:	n/a
28	chr11:18141393-18141443	PrEC	prostate:	n/a
29	chr11:18141625-18141675	K562	blood:	n/a
30	chr11:18138394-18138444	GM12878	blood:	n/a
31	chr11:18138394-18138444	IMR90	lung:	fetal
32	chr11:18139019-18139069	K562	blood:	n/a
33	chr11:18138837-18138887	GM12892	blood:	n/a
34	chr11:18141393-18141443	PFSK-1	brain:	n/a
35	chr11:18139019-18139069	MCF10A-Er-Src	breast:	n/a
36	chr11:18141625-18141675	NH-A	brain:	n/a
37	chr11:18138837-18138887	HCPEpiC	choroid plexus:	n/a
38	chr11:18139019-18139069	Jurkat	blood:	n/a
39	chr11:18138394-18138444	NB4	blood:	n/a
40	chr11:18141393-18141443	MCF10A-Er-Src	breast:	n/a
41	chr11:18141625-18141675	IMR90	lung:	fetal
42	chr11:18141393-18141443	GM19239	blood:	n/a
43	chr11:18141393-18141443	HRCEpiC	kidney:	n/a
44	chr11:18138394-18138444	Hepatocyte	liver:	n/a
45	chr11:18139019-18139069	GM12891	blood:	n/a
46	chr11:18139019-18139069	HEK293	kidney:	embryo
47	chr11:18141393-18141443	AG04449	skin:	fetal
48	chr11:18138837-18138887	AG04450	lung:	fetal
49	chr11:18137155-18137205	NHBE	bronchial:	n/a
50	chr11:18139019-18139069	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:18129937..18132651-chr11:18134696..18136776,2	K562	blood:
2	chr11:18126382..18129107-chr11:18133072..18137043,3	K562	blood:
3	chr11:18126284..18129283-chr11:18131748..18134155,2	MCF-7	breast:
4	chr11:18129937..18132651-chr11:18134696..18136776,2	K562	blood:
5	chr11:18127813..18129704-chr11:18132891..18135867,2	MCF-7	breast:
6	chr11:18127425..18129160-chr11:18131186..18134005,2	K562	blood:
7	chr11:18152566..18154757-chr11:18415660..18417661,2	K562	blood:
8	chr11:18031292..18032013-chr11:18136940..18137699,2	MCF-7	breast:
9	chr11:18127466..18129015-chr11:18138742..18140750,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAAL1-1	chr11:18134173-18134308	NONHSAT018263
2	lnc-SAAL1-1	chr11:18134699-18134839	NONHSAT018263
3	lnc-SAAL1-1	chr11:18137538-18137625	NONHSAT018263

Variant related genes	Relation type
MRGPRX3	TF binding region
SAA3P	TF binding region
SAAL1	TF binding region
MRGPRX3	CpG island
SAA3P	CpG island
SAAL1	CpG island
ENSG00000166788	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000129158	chromatin interactions
ENSG00000255254	chromatin interactions

Extended variants
information (count: 632 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372511247	chr11:18132219-18132220	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs149168337	chr11:18132228-18132229	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs532331980	chr11:18132248-18132249	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs191044760	chr11:18132249-18132250	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs182987383	chr11:18132297-18132298	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs143229396	chr11:18132298-18132299	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576255679	chr11:18132317-18132318	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs187537379	chr11:18132318-18132319	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs566632248	chr11:18132336-18132337	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs375577757	chr11:18132384-18132385	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs533994908	chr11:18132393-18132394	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs78180763	chr11:18132400-18132401	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs148306235	chr11:18132432-18132433	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs373911412	chr11:18132470-18132471	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs554224380	chr11:18132554-18132555	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs572796229	chr11:18132561-18132562	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs191225423	chr11:18132599-18132600	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs142242382	chr11:18132622-18132623	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs560010852	chr11:18132675-18132676	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573064630	chr11:18132681-18132682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183342928	chr11:18132683-18132684	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs61882532	chr11:18132706-18132707	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532712576	chr11:18132716-18132717	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187731011	chr11:18132724-18132725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs16934947	chr11:18132732-18132733	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35861522	chr11:18132785-18132786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138485600	chr11:18132808-18132809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192159820	chr11:18132812-18132813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553669235	chr11:18132817-18132818	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375322949	chr11:18132819-18132820	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566861705	chr11:18132829-18132830	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368631057	chr11:18132850-18132851	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142909762	chr11:18132851-18132852	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185051715	chr11:18132852-18132853	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188315373	chr11:18132915-18132916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538178768	chr11:18132920-18132921	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555861648	chr11:18132969-18132970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs539891074	chr11:18132998-18132999	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574345381	chr11:18133025-18133026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs907922	chr11:18133042-18133043	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs146129519	chr11:18133053-18133054	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571810855	chr11:18133069-18133070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192646173	chr11:18133093-18133094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540423394	chr11:18133102-18133103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565804615	chr11:18133170-18133171	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369482864	chr11:18133197-18133198	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139074610	chr11:18133205-18133206	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577100700	chr11:18133226-18133227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376136115	chr11:18133269-18133270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs67231939	chr11:18133277-18133278	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18128400-18137400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:18129000-18139000	Weak transcription	Right Atrium	heart
3	chr11:18134600-18134800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:18134800-18137200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:18136600-18141600	Enhancers	HepG2	liver
6	chr11:18136800-18137000	Enhancers	Dnd41	blood
7	chr11:18136800-18137200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:18136800-18137400	Enhancers	Hela-S3	cervix
9	chr11:18136800-18137600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:18136800-18139800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:18136800-18141600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:18137000-18137200	Enhancers	Brain Hippocampus Middle	brain
13	chr11:18137000-18137200	Flanking Active TSS	Dnd41	blood
14	chr11:18137000-18137200	Enhancers	GM12878-XiMat	blood
15	chr11:18137000-18137400	Enhancers	Primary B cells from peripheral blood	blood
16	chr11:18137000-18137400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr11:18137000-18137400	Enhancers	Brain Angular Gyrus	brain
18	chr11:18137000-18137400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr11:18137000-18137400	Enhancers	Stomach Mucosa	stomach
20	chr11:18137000-18137600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
21	chr11:18137000-18137600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:18137000-18137600	Enhancers	Liver	Liver
23	chr11:18137000-18137600	Enhancers	Duodenum Mucosa	Duodenum
24	chr11:18137200-18137400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:18137200-18137400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr11:18137200-18137400	Enhancers	Gastric	stomach
27	chr11:18137200-18137400	Enhancers	Ovary	ovary
28	chr11:18137200-18137400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
29	chr11:18137200-18137600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr11:18137200-18137600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr11:18137200-18137600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr11:18137200-18137600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:18137200-18137600	Enhancers	Dnd41	blood
34	chr11:18137400-18138200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:18137400-18141600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:18138200-18138400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:18138200-18140200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr11:18138400-18139200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:18139000-18139600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr11:18139200-18139600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:18139200-18140000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:18141600-18142800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:18141600-18143600	Weak transcription	HepG2	liver
44	chr11:18141600-18143800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr11:18142800-18144200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:18143600-18144200	Enhancers	HepG2	liver
47	chr11:18143800-18144000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr11:18150200-18150400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:18150400-18156200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:18151800-18154200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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