Variant report

Variant	nsv1040140
Chromosome Location	chr15:45121635-45289756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1300)
CpG islands
(count:366)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45205265-45205621	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:45145528-45145856	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:45123189-45123508	K562	blood:	n/a	n/a
4	ARID3A	chr15:45271890-45272170	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:45128282-45128791	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:45125283-45125468	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:45181194-45181211	K562	blood:	n/a	n/a
8	ARID3A	chr15:45123098-45123535	HepG2	liver:	n/a	n/a
9	ATF1	chr15:45182020-45182040	K562	blood:	n/a	n/a
10	ATF1	chr15:45168202-45168273	K562	blood:	n/a	n/a
11	ATF1	chr15:45145566-45145860	K562	blood:	n/a	n/a
12	ATF1	chr15:45123175-45123515	K562	blood:	n/a	n/a
13	ATF2	chr15:45203385-45203780	GM12878	blood:	n/a	n/a
14	ATF2	chr15:45203414-45203775	GM12878	blood:	n/a	n/a
15	ATF2	chr15:45174666-45175297	GM12878	blood:	n/a	n/a
16	ATF2	chr15:45174555-45175594	GM12878	blood:	n/a	n/a
17	BACH1	chr15:45146115-45146175	K562	blood:	n/a	n/a
18	BATF	chr15:45279851-45280251	GM12878	blood:	n/a	n/a
19	BATF	chr15:45214951-45215126	GM12878	blood:	n/a	n/a
20	BATF	chr15:45175615-45176106	GM12878	blood:	n/a	n/a
21	BATF	chr15:45260122-45260297	GM12878	blood:	n/a	n/a
22	BATF	chr15:45131166-45131498	GM12878	blood:	n/a	n/a
23	BATF	chr15:45131114-45131510	GM12878	blood:	n/a	n/a
24	BATF	chr15:45203489-45203757	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
25	BATF	chr15:45191947-45192347	GM12878	blood:	n/a	n/a
26	BATF	chr15:45203408-45203799	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
27	BATF	chr15:45174500-45176189	GM12878	blood:	n/a	n/a
28	BATF	chr15:45191999-45192251	GM12878	blood:	n/a	n/a
29	BATF	chr15:45272154-45272541	GM12878	blood:	n/a	chr15:45272467-45272476
30	BATF	chr15:45279994-45280199	GM12878	blood:	n/a	n/a
31	BATF	chr15:45145545-45145867	GM12878	blood:	n/a	n/a
32	BATF	chr15:45204924-45205158	GM12878	blood:	n/a	chr15:45204943-45204952
33	BATF	chr15:45174732-45175340	GM12878	blood:	n/a	n/a
34	BATF	chr15:45272208-45272505	GM12878	blood:	n/a	chr15:45272467-45272476
35	BCL11A	chr15:45174655-45175245	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:45131165-45131444	GM12878	blood:	n/a	chr15:45131356-45131365
37	BCL11A	chr15:45272182-45272561	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:45175417-45176211	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:45191932-45192270	GM12878	blood:	n/a	n/a
40	BCL11A	chr15:45272174-45272394	GM12878	blood:	n/a	n/a
41	BCL11A	chr15:45279928-45280266	GM12878	blood:	n/a	n/a
42	BCL11A	chr15:45175527-45176004	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:45203459-45203776	GM12878	blood:	n/a	chr15:45203595-45203604 chr15:45203594-45203603
44	BCL11A	chr15:45137220-45137412	GM12878	blood:	n/a	n/a
45	BCL11A	chr15:45174637-45175348	GM12878	blood:	n/a	n/a
46	BCL3	chr15:45174662-45175296	GM12878	blood:	n/a	n/a
47	BCLAF1	chr15:45173453-45173866	GM12878	blood:	n/a	n/a
48	BCLAF1	chr15:45174315-45175214	GM12878	blood:	n/a	n/a
49	BCLAF1	chr15:45174481-45175331	GM12878	blood:	n/a	n/a
50	BCLAF1	chr15:45145496-45145860	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45248463-45248513	SKMC	muscle:	n/a
2	chr15:45248806-45248856	PFSK-1	brain:	n/a
3	chr15:45248806-45248856	AG04450	lung:	fetal
4	chr15:45248932-45248982	SAEC	small airway:	n/a
5	chr15:45247870-45247920	PANC-1	pancreas:	n/a
6	chr15:45248463-45248513	NT2-D1	testis:	n/a
7	chr15:45248878-45248928	H1-hESC	embryonic stem cell:	embryo
8	chr15:45248806-45248856	CMK	blood:	n/a
9	chr15:45248744-45248794	ProgFib	skin:	n/a
10	chr15:45248932-45248982	BE2_C	brain:	n/a
11	chr15:45248878-45248928	AG09319	gingival:	n/a
12	chr15:45248744-45248794	AG04449	skin:	fetal
13	chr15:45248878-45248928	HRPEpiC	eye:	n/a
14	chr15:45247870-45247920	AG04450	lung:	fetal
15	chr15:45248878-45248928	U87	brain:	n/a
16	chr15:45247870-45247920	GM19239	blood:	n/a
17	chr15:45248463-45248513	HNPCEpiC	eye:	n/a
18	chr15:45247870-45247920	ECC-1	luminal epithelium:	n/a
19	chr15:45248744-45248794	HEEpiC	esophagus:	n/a
20	chr15:45248744-45248794	SK-N-SH_RA	brain:	n/a
21	chr15:45247870-45247920	HAEpiC	amniotic membrane:	n/a
22	chr15:45248463-45248513	Jurkat	blood:	n/a
23	chr15:45248806-45248856	BE2_C	brain:	n/a
24	chr15:45248463-45248513	HRE	kidney:	n/a
25	chr15:45248932-45248982	K562	blood:	n/a
26	chr15:45247870-45247920	HUVEC	blood vessel:	n/a
27	chr15:45248744-45248794	HCF	heart:	n/a
28	chr15:45247870-45247920	SK-N-SH_RA	brain:	n/a
29	chr15:45248463-45248513	AG09319	gingival:	n/a
30	chr15:45248806-45248856	GM12892	blood:	n/a
31	chr15:45248878-45248928	NB4	blood:	n/a
32	chr15:45248744-45248794	HCPEpiC	choroid plexus:	n/a
33	chr15:45248744-45248794	LNCaP	prostate:	n/a
34	chr15:45248806-45248856	NHBE	bronchial:	n/a
35	chr15:45248744-45248794	U87	brain:	n/a
36	chr15:45248878-45248928	GM12892	blood:	n/a
37	chr15:45248878-45248928	HCT-116	colon:	n/a
38	chr15:45248744-45248794	HCT-116	colon:	n/a
39	chr15:45248806-45248856	NB4	blood:	n/a
40	chr15:45248744-45248794	Hepatocyte	liver:	n/a
41	chr15:45248806-45248856	Jurkat	blood:	n/a
42	chr15:45248932-45248982	HCPEpiC	choroid plexus:	n/a
43	chr15:45248463-45248513	NHDF-neo	bronchial:	n/a
44	chr15:45248744-45248794	GM12891	blood:	n/a
45	chr15:45248932-45248982	Hela-S3	cervix:	n/a
46	chr15:45248878-45248928	GM12891	blood:	n/a
47	chr15:45248744-45248794	MCF-7	breast:	n/a
48	chr15:45248806-45248856	ECC-1	luminal epithelium:	n/a
49	chr15:45247870-45247920	SAEC	small airway:	n/a
50	chr15:45248878-45248928	HCF	heart:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45264164..45266093-chr15:45270183..45271983,2	K562	blood:
2	chr15:45153661..45154310-chr15:45315073..45315837,2	NB4	blood:
3	chr15:45003163..45005190-chr15:45225441..45227864,2	K562	blood:
4	chr15:45145307..45146142-chr15:45409718..45410518,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf43-2	chr15:45174295-45174981	NONHSAT042199
2	lnc-C15orf43-1	chr15:45211574-45211851	NONHSAT042202
3	lnc-DUOX2-4	chr15:45262233-45263376	NONHSAT042205
4	lnc-C15orf43-1	chr15:45212156-45213018	NONHSAT042202

No data

Variant related genes	Relation type
ENSG00000259479	TF binding region
RNU6-966P	TF binding region
C15orf43	TF binding region
RNU6-1332P	TF binding region
ENSG00000238845	TF binding region
RNU1-119P	TF binding region
ENSG00000259742	TF binding region
ENSG00000259304	TF binding region
RNU6-1108P	TF binding region
ENSG00000259231	TF binding region
ENSG00000259479	CpG island
RNU6-966P	CpG island
C15orf43	CpG island
RNU6-1332P	CpG island
ENSG00000238845	CpG island
RNU1-119P	CpG island
ENSG00000259742	CpG island
ENSG00000259304	CpG island
RNU6-1108P	CpG island
ENSG00000259231	CpG island
ENSG00000252288	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000229474	chromatin interactions
ENSG00000140263	chromatin interactions

Extended variants
information (count: 3609 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3609 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4776211	chr15:45121635-45121636	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150891931	chr15:45121657-45121658	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542358327	chr15:45121669-45121670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562117964	chr15:45121671-45121672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112652480	chr15:45121672-45121673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540909236	chr15:45121717-45121718	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs372316888	chr15:45121760-45121761	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564291525	chr15:45121769-45121770	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs533106686	chr15:45121795-45121796	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs191061592	chr15:45121799-45121800	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2689316	chr15:45121804-45121805	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145544596	chr15:45121841-45121842	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs147600825	chr15:45121863-45121864	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs2689315	chr15:45121890-45121891	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs548669330	chr15:45121912-45121913	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs149675564	chr15:45121921-45121922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369538155	chr15:45121935-45121936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2261442	chr15:45121946-45121947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377548726	chr15:45121986-45121987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2689313	chr15:45122026-45122027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553890155	chr15:45122027-45122028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554103659	chr15:45122030-45122031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572252638	chr15:45122080-45122081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539764688	chr15:45122083-45122084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556861109	chr15:45122092-45122093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576508332	chr15:45122102-45122103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141055244	chr15:45122172-45122173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555789502	chr15:45122178-45122179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201929138	chr15:45122222-45122223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369742674	chr15:45122223-45122224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138351871	chr15:45122224-45122225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541495110	chr15:45122225-45122226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140998114	chr15:45122240-45122241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533117836	chr15:45122254-45122255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543323870	chr15:45122284-45122285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202219400	chr15:45122318-45122319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529145693	chr15:45122446-45122447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs183645260	chr15:45122451-45122452	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561953510	chr15:45122482-45122483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs565652351	chr15:45122521-45122522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149339450	chr15:45122546-45122547	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs528202064	chr15:45122586-45122587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs529286273	chr15:45122587-45122588	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs28409579	chr15:45122608-45122609	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs570970641	chr15:45122628-45122629	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544742973	chr15:45122728-45122729	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs556793687	chr15:45122760-45122761	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562965530	chr15:45122763-45122764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs536139873	chr15:45122767-45122768	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs186355588	chr15:45122798-45122799	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45112000-45123000	Weak transcription	Esophagus	oesophagus
2	chr15:45117600-45121800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr15:45118400-45123000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr15:45119800-45123000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:45120400-45121800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:45120400-45122000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr15:45120400-45125200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:45120400-45128400	Weak transcription	Spleen	Spleen
9	chr15:45120600-45122000	Enhancers	Brain Cingulate Gyrus	brain
10	chr15:45120600-45124000	Enhancers	Pancreas	Pancrea
11	chr15:45120800-45122000	Weak transcription	Lung	lung
12	chr15:45120800-45123200	Weak transcription	Placenta	Placenta
13	chr15:45120800-45123400	Weak transcription	Liver	Liver
14	chr15:45120800-45129400	Enhancers	HepG2	liver
15	chr15:45120800-45131800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr15:45121200-45123800	Enhancers	Stomach Mucosa	stomach
17	chr15:45121200-45124600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr15:45121400-45121800	Enhancers	Brain Anterior Caudate	brain
19	chr15:45121400-45122000	Enhancers	Brain Substantia Nigra	brain
20	chr15:45121400-45122000	Enhancers	K562	blood
21	chr15:45121400-45122200	Enhancers	Brain Hippocampus Middle	brain
22	chr15:45121400-45122200	Enhancers	Gastric	stomach
23	chr15:45121400-45122200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr15:45121400-45125200	Enhancers	Fetal Thymus	thymus
25	chr15:45121600-45122000	Enhancers	Brain Angular Gyrus	brain
26	chr15:45121600-45122000	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr15:45121600-45122200	Enhancers	Fetal Intestine Small	intestine
28	chr15:45121600-45123200	Enhancers	Dnd41	blood
29	chr15:45121800-45123800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr15:45121800-45123800	Enhancers	Fetal Intestine Large	intestine
31	chr15:45121800-45124600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr15:45122000-45122200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:45122000-45122200	Enhancers	Lung	lung
34	chr15:45122000-45123000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr15:45122000-45123000	Weak transcription	K562	blood
36	chr15:45122000-45123200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr15:45122200-45122600	Weak transcription	Fetal Intestine Small	intestine
38	chr15:45122200-45122600	Weak transcription	Lung	lung
39	chr15:45122200-45123200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr15:45122200-45123200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr15:45122600-45123200	Enhancers	Lung	lung
42	chr15:45122600-45123600	Enhancers	Fetal Intestine Small	intestine
43	chr15:45122600-45123800	Enhancers	Duodenum Mucosa	Duodenum
44	chr15:45122600-45123800	Enhancers	HMEC	breast
45	chr15:45122800-45123400	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr15:45122800-45123400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr15:45122800-45123600	Enhancers	Primary T cells fromperipheralblood	blood
48	chr15:45122800-45123800	Enhancers	Hela-S3	cervix
49	chr15:45122800-45123800	Enhancers	NHEK	skin
50	chr15:45122800-45124000	Enhancers	HUVEC	blood vessel

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