Variant report

Variant	nsv817693
Chromosome Location	chr15:55788832-55809660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:977)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55790421-55790685	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:55806152-55806285	K562	blood:	n/a	n/a
3	BACH1	chr15:55790323-55790739	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:55790292-55790938	A549	lung:	n/a	n/a
5	BCL3	chr15:55790199-55790921	A549	lung:	n/a	n/a
6	BHLHE40	chr15:55790520-55790743	K562	blood:	n/a	n/a
7	BHLHE40	chr15:55802897-55803042	K562	blood:	n/a	n/a
8	BHLHE40	chr15:55790404-55790780	HepG2	liver:	n/a	n/a
9	BHLHE40	chr15:55791493-55791621	A549	lung:	n/a	n/a
10	BHLHE40	chr15:55790324-55790820	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:55790144-55790756	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr15:55790508-55790732	K562	blood:	n/a	n/a
13	CEBPB	chr15:55790197-55790762	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr15:55790301-55790641	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr15:55790376-55790772	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr15:55790547-55790664	K562	blood:	n/a	n/a
17	CHD2	chr15:55790494-55790782	HepG2	liver:	n/a	n/a
18	CHD2	chr15:55790264-55790852	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr15:55790251-55790891	A549	lung:	n/a	n/a
20	CREB1	chr15:55790318-55790783	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr15:55806105-55806345	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:55806160-55806310	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:55806180-55806330	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr15:55806160-55806310	GM12865	blood:	n/a	n/a
25	CTCF	chr15:55806080-55806230	RPTEC	kidney:	n/a	n/a
26	CTCF	chr15:55806140-55806290	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr15:55806125-55806333	A549	lung:	n/a	n/a
28	CTCF	chr15:55806159-55806321	GM20000	blood:	n/a	n/a
29	CTCF	chr15:55806140-55806290	GM12872	blood:	n/a	n/a
30	CTCF	chr15:55806140-55806290	GM12866	blood:	n/a	n/a
31	CTCF	chr15:55806192-55806335	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr15:55806140-55806290	NHEK	skin:	n/a	n/a
33	CTCF	chr15:55806195-55806283	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:55806123-55806334	ProgFib	skin:	n/a	n/a
35	CTCF	chr15:55806180-55806330	AG04449	skin:	n/a	n/a
36	CTCF	chr15:55806160-55806310	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr15:55806066-55806420	K562	blood:	n/a	n/a
38	CTCF	chr15:55806180-55806330	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr15:55806140-55806290	HAc	cerebellar:	n/a	n/a
40	CTCF	chr15:55806160-55806310	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr15:55806160-55806310	NHLF	lung:	n/a	n/a
42	CTCF	chr15:55806092-55806341	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr15:55790440-55790590	GM12864	blood:	n/a	n/a
44	CTCF	chr15:55806123-55806332	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr15:55806180-55806330	RPTEC	kidney:	n/a	n/a
46	CTCF	chr15:55806100-55806250	HFF	foreskin:	n/a	n/a
47	CTCF	chr15:55806160-55806310	GM06990	blood:	n/a	n/a
48	CTCF	chr15:55806169-55806283	GM12891	blood:	n/a	n/a
49	CTCF	chr15:55806220-55806370	GM12868	blood:	n/a	n/a
50	CTCF	chr15:55806178-55806297	SK-N-SH_RA	brain:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55790571-55790621	HIPEpiC	eye:	n/a
2	chr15:55790571-55790621	HIPEpiC	eye:	n/a
3	chr15:55791821-55791871	HCF	heart:	n/a
4	chr15:55790753-55790803	HMEC	breast:	n/a
5	chr15:55790509-55790559	NH-A	brain:	n/a
6	chr15:55801378-55801428	NHDF-neo	bronchial:	n/a
7	chr15:55800831-55800881	GM06990	blood:	n/a
8	chr15:55790753-55790803	Hepatocyte	liver:	n/a
9	chr15:55805949-55805999	HEEpiC	esophagus:	n/a
10	chr15:55805949-55805999	Hepatocyte	liver:	n/a
11	chr15:55793864-55793914	SKMC	muscle:	n/a
12	chr15:55805566-55805616	NH-A	brain:	n/a
13	chr15:55790571-55790621	LNCaP	prostate:	n/a
14	chr15:55805949-55805999	ovcar-3	ovarian:	n/a
15	chr15:55790675-55790725	HIPEpiC	eye:	n/a
16	chr15:55805566-55805616	NHDF-neo	bronchial:	n/a
17	chr15:55793864-55793914	SK-N-MC	brain:	n/a
18	chr15:55805566-55805616	BE2_C	brain:	n/a
19	chr15:55790675-55790725	SK-N-MC	brain:	n/a
20	chr15:55790608-55790658	AG04449	skin:	fetal
21	chr15:55805949-55805999	HCT-116	colon:	n/a
22	chr15:55805566-55805616	A549	lung:	n/a
23	chr15:55790675-55790725	HNPCEpiC	eye:	n/a
24	chr15:55790509-55790559	BE2_C	brain:	n/a
25	chr15:55790509-55790559	HEK293	kidney:	embryo
26	chr15:55790571-55790621	MCF-7	breast:	n/a
27	chr15:55799927-55799977	SKMC	muscle:	n/a
28	chr15:55800831-55800881	HEEpiC	esophagus:	n/a
29	chr15:55790675-55790725	U87	brain:	n/a
30	chr15:55791821-55791871	GM12891	blood:	n/a
31	chr15:55793864-55793914	NH-A	brain:	n/a
32	chr15:55801378-55801428	Hepatocyte	liver:	n/a
33	chr15:55800831-55800881	IMR90	lung:	fetal
34	chr15:55790446-55790496	SAEC	small airway:	n/a
35	chr15:55790509-55790559	SAEC	small airway:	n/a
36	chr15:55790571-55790621	NB4	blood:	n/a
37	chr15:55800831-55800881	HEK293	kidney:	embryo
38	chr15:55799927-55799977	Jurkat	blood:	n/a
39	chr15:55805566-55805616	GM12891	blood:	n/a
40	chr15:55801378-55801428	RPTEC	kidney:	n/a
41	chr15:55801378-55801428	HMEC	breast:	n/a
42	chr15:55790509-55790559	A549	lung:	n/a
43	chr15:55790446-55790496	HRCEpiC	kidney:	n/a
44	chr15:55805566-55805616	HRE	kidney:	n/a
45	chr15:55806536-55806586	NHDF-neo	bronchial:	n/a
46	chr15:55806536-55806586	ECC-1	luminal epithelium:	n/a
47	chr15:55801378-55801428	Jurkat	blood:	n/a
48	chr15:55790753-55790803	T-47D	breast:	n/a
49	chr15:55801378-55801428	Hela-S3	cervix:	n/a
50	chr15:55805949-55805999	HIPEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:55805811..55806979-chr15:55933287..55934076,3	MCF-7	breast:
2	chr1:222884982..222885886-chr15:55790504..55791243,2	Hela-S3	cervix:
3	chr15:55609486..55611262-chr15:55788891..55791859,2	K562	blood:
4	chr15:55789676..55792813-chr15:55797068..55799898,3	MCF-7	breast:
5	chr15:55790459..55791055-chr21:48054984..48055756,2	HCT-116	colon:
6	chr15:55808580..55811274-chr15:55928806..55931409,2	MCF-7	breast:

No data

Variant related genes	Relation type
DYX1C1-CCPG1	TF binding region
DYX1C1	TF binding region
DYX1C1-CCPG1	CpG island
DYX1C1	CpG island
ENSG00000160310	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000186063	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000256061	chromatin interactions

Extended variants
information (count: 822 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16976351	chr15:55788832-55788833	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544149802	chr15:55788880-55788881	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs35358181	chr15:55788942-55788943	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs530968229	chr15:55788952-55788953	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185672117	chr15:55788996-55788997	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190187681	chr15:55789015-55789016	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181872799	chr15:55789037-55789038	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531341554	chr15:55789084-55789085	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs529489921	chr15:55789104-55789105	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183973794	chr15:55789161-55789162	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545079385	chr15:55789194-55789195	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79593205	chr15:55789216-55789217	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114925350	chr15:55789287-55789288	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs574435484	chr15:55789293-55789294	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188350259	chr15:55789294-55789295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs116283981	chr15:55789295-55789296	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565031942	chr15:55789306-55789307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144827921	chr15:55789469-55789470	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12594443	chr15:55789478-55789479	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546478863	chr15:55789571-55789572	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559993496	chr15:55789654-55789655	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147950047	chr15:55789655-55789656	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376217179	chr15:55789658-55789659	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551201977	chr15:55789666-55789667	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs367890935	chr15:55789688-55789689	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs547596578	chr15:55789700-55789701	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs112801701	chr15:55789704-55789705	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530880617	chr15:55789720-55789721	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550965003	chr15:55789734-55789735	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564279887	chr15:55789788-55789789	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112865941	chr15:55789794-55789795	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529901477	chr15:55789830-55789831	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549671566	chr15:55789844-55789845	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570840967	chr15:55789845-55789846	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552098174	chr15:55789849-55789850	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77409626	chr15:55789866-55789867	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369963647	chr15:55789867-55789868	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs17819126	chr15:55789910-55789911	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548061833	chr15:55789915-55789916	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568171906	chr15:55789938-55789939	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149208897	chr15:55789947-55789948	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143352613	chr15:55789966-55789967	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114245686	chr15:55789984-55789985	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142108738	chr15:55789995-55789996	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373804332	chr15:55790001-55790002	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs145868397	chr15:55790012-55790013	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138697313	chr15:55790037-55790038	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376383092	chr15:55790046-55790047	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs61733359	chr15:55790053-55790054	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576862642	chr15:55790118-55790119	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55756200-55790000	Weak transcription	Fetal Kidney	kidney
2	chr15:55771400-55790000	Weak transcription	HSMM	muscle
3	chr15:55771600-55790000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr15:55772200-55790000	Weak transcription	Brain Angular Gyrus	brain
5	chr15:55772800-55789800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:55773800-55790200	Weak transcription	Pancreas	Pancrea
7	chr15:55774000-55790000	Weak transcription	Fetal Heart	heart
8	chr15:55774200-55790200	Weak transcription	Lung	lung
9	chr15:55774400-55789800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr15:55774400-55790000	Weak transcription	Brain Hippocampus Middle	brain
11	chr15:55774400-55790200	Weak transcription	Gastric	stomach
12	chr15:55774600-55789800	Weak transcription	Colon Smooth Muscle	Colon
13	chr15:55774800-55789600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr15:55774800-55789600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr15:55775000-55789600	Weak transcription	Fetal Brain Male	brain
16	chr15:55775200-55789800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr15:55775200-55789800	Weak transcription	Brain Germinal Matrix	brain
18	chr15:55775200-55789800	Weak transcription	Fetal Lung	lung
19	chr15:55779600-55789400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr15:55779600-55789800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr15:55779600-55789800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr15:55779600-55790000	Weak transcription	Adipose Nuclei	Adipose
23	chr15:55779600-55790000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr15:55779800-55789800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:55779800-55790200	Weak transcription	Fetal Muscle Leg	muscle
26	chr15:55780000-55789600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:55780000-55790000	Weak transcription	Fetal Intestine Small	intestine
28	chr15:55780000-55790200	Weak transcription	Aorta	Aorta
29	chr15:55780000-55790200	Weak transcription	Left Ventricle	heart
30	chr15:55780400-55790000	Weak transcription	Ovary	ovary
31	chr15:55780600-55789400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:55780600-55789800	Weak transcription	Fetal Brain Female	brain
33	chr15:55780800-55789800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr15:55781000-55789800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr15:55781200-55789800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr15:55781600-55789400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr15:55781600-55789800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:55781600-55789800	Weak transcription	Osteobl	bone
39	chr15:55781800-55789400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:55781800-55789800	Weak transcription	Fetal Intestine Large	intestine
41	chr15:55781800-55790000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:55782000-55789800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:55782000-55789800	Weak transcription	A549	lung
44	chr15:55782800-55790000	Weak transcription	HSMMtube	muscle
45	chr15:55783000-55790000	Weak transcription	Brain Substantia Nigra	brain
46	chr15:55783600-55789600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:55783800-55789800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:55785400-55790000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr15:55785400-55790000	Weak transcription	Stomach Smooth Muscle	stomach
50	chr15:55785600-55789800	Weak transcription	Brain Anterior Caudate	brain

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