Variant report

Variant	nsv984091
Chromosome Location	chr15:74640375-74659005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:611)
Chromatin interactive
region (count:7)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:74657670-74658074	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr15:74651781-74652041	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:74657887-74658256	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr15:74657769-74658026	HepG2	liver:	n/a	n/a
5	BRCA1	chr15:74657799-74658673	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr15:74646173-74646445	K562	blood:	n/a	n/a
7	CBX3	chr15:74646265-74646464	K562	blood:	n/a	n/a
8	CCNT2	chr15:74658041-74658147	K562	blood:	n/a	n/a
9	CEBPB	chr15:74651813-74651942	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr15:74653307-74653601	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr15:74642726-74642926	K562	blood:	n/a	n/a
12	CEBPB	chr15:74651954-74651980	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:74649871-74650178	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr15:74642703-74642956	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:74652339-74652875	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:74642801-74642924	IMR90	lung:	n/a	n/a
17	CEBPB	chr15:74657579-74658706	Hela-S3	cervix:	n/a	n/a
18	CHD1	chr15:74658179-74658186	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:74657405-74658677	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr15:74657259-74657450	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:74658087-74658199	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr15:74657673-74658494	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr15:74657699-74658750	HepG2	liver:	n/a	n/a
24	CREB1	chr15:74657790-74658743	HepG2	liver:	n/a	n/a
25	CREB1	chr15:74657793-74658431	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr15:74649088-74649127	LNCaP	prostate:	n/a	n/a
27	CTCF	chr15:74658140-74658290	AG09309	skin:	n/a	n/a
28	CTCF	chr15:74658060-74658210	BJ	skin:	n/a	n/a
29	CTCF	chr15:74658136-74658266	ProgFib	skin:	n/a	n/a
30	CTCF	chr15:74658080-74658230	GM12874	blood:	n/a	n/a
31	CTCF	chr15:74658120-74658270	GM06990	blood:	n/a	n/a
32	CTCF	chr15:74641440-74641590	GM12872	blood:	n/a	n/a
33	CTCF	chr15:74658100-74658250	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr15:74658080-74658230	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr15:74658140-74658290	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr15:74658195-74658316	GM10266	blood:	n/a	n/a
37	CTCF	chr15:74658140-74658290	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr15:74641317-74641361	GM20000	blood:	n/a	n/a
39	CTCF	chr15:74658140-74658290	AG04449	skin:	n/a	n/a
40	CTCF	chr15:74658220-74658370	SAEC	small airway:	n/a	n/a
41	CTCF	chr15:74658060-74658210	HRE	kidney:	n/a	n/a
42	CTCF	chr15:74655706-74655765	GM13976	blood:	n/a	n/a
43	CTCF	chr15:74658140-74658290	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr15:74658200-74658350	BJ	skin:	n/a	n/a
45	CTCF	chr15:74658060-74658210	HepG2	liver:	n/a	n/a
46	CTCF	chr15:74658191-74658292	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:74658340-74658490	AG04449	skin:	n/a	n/a
48	CTCF	chr15:74658120-74658270	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr15:74658060-74658210	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr15:74658100-74658250	HBMEC	blood vessel:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74658653-74658703	HEK293	kidney:	embryo
2	chr15:74658653-74658703	HEK293	kidney:	embryo
3	chr15:74658981-74659031	GM12892	blood:	n/a
4	chr15:74658573-74658623	HCT-116	colon:	n/a
5	chr15:74645873-74645923	HAEpiC	amniotic membrane:	n/a
6	chr15:74658244-74658294	GM12891	blood:	n/a
7	chr15:74658166-74658216	HL-60	blood:	n/a
8	chr15:74658573-74658623	U87	brain:	n/a
9	chr15:74658244-74658294	U87	brain:	n/a
10	chr15:74658166-74658216	HEEpiC	esophagus:	n/a
11	chr15:74658547-74658597	Caco-2	colon:	n/a
12	chr15:74657911-74657961	IMR90	lung:	fetal
13	chr15:74658981-74659031	SK-N-MC	brain:	n/a
14	chr15:74645873-74645923	HNPCEpiC	eye:	n/a
15	chr15:74658553-74658603	Hela-S3	cervix:	n/a
16	chr15:74658653-74658703	AG09319	gingival:	n/a
17	chr15:74658981-74659031	BJ	skin:	n/a
18	chr15:74658244-74658294	HEK293	kidney:	embryo
19	chr15:74658981-74659031	HCM	heart:	n/a
20	chr15:74658553-74658603	H1-hESC	embryonic stem cell:	embryo
21	chr15:74658573-74658623	HNPCEpiC	eye:	n/a
22	chr15:74658244-74658294	HL-60	blood:	n/a
23	chr15:74658653-74658703	HCT-116	colon:	n/a
24	chr15:74658547-74658597	HAEpiC	amniotic membrane:	n/a
25	chr15:74658330-74658380	HCF	heart:	n/a
26	chr15:74658653-74658703	ovcar-3	ovarian:	n/a
27	chr15:74658553-74658603	ECC-1	luminal epithelium:	n/a
28	chr15:74658166-74658216	AG04450	lung:	fetal
29	chr15:74658573-74658623	T-47D	breast:	n/a
30	chr15:74658653-74658703	GM12892	blood:	n/a
31	chr15:74658244-74658294	K562	blood:	n/a
32	chr15:74645873-74645923	AG04449	skin:	fetal
33	chr15:74658547-74658597	HEEpiC	esophagus:	n/a
34	chr15:74658330-74658380	PFSK-1	brain:	n/a
35	chr15:74645873-74645923	T-47D	breast:	n/a
36	chr15:74658573-74658623	PrEC	prostate:	n/a
37	chr15:74658573-74658623	HRE	kidney:	n/a
38	chr15:74658653-74658703	NB4	blood:	n/a
39	chr15:74658981-74659031	HCT-116	colon:	n/a
40	chr15:74645873-74645923	K562	blood:	n/a
41	chr15:74658166-74658216	AG09319	gingival:	n/a
42	chr15:74658330-74658380	Hela-S3	cervix:	n/a
43	chr15:74658573-74658623	AG04450	lung:	fetal
44	chr15:74658553-74658603	HEEpiC	esophagus:	n/a
45	chr15:74658547-74658597	Jurkat	blood:	n/a
46	chr15:74658244-74658294	PrEC	prostate:	n/a
47	chr15:74658653-74658703	GM12878	blood:	n/a
48	chr15:74658553-74658603	GM12878	blood:	n/a
49	chr15:74658547-74658597	NT2-D1	testis:	n/a
50	chr15:74658553-74658603	AG09319	gingival:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:128593900..128594524-chr15:74657844..74658595,3	Hela-S3	cervix:
2	chr15:74635843..74637351-chr15:74638893..74640725,2	MCF-7	breast:
3	chr1:186344109..186344880-chr15:74657844..74658592,2	Hela-S3	cervix:
4	chr15:74656941..74659751-chr15:74906408..74907911,2	MCF-7	breast:
5	chr15:74638641..74640851-chr15:74642366..74644922,2	K562	blood:
6	chr15:74658083..74658610-chr17:74722803..74723636,2	Hela-S3	cervix:
7	chr1:45196380..45197273-chr15:74657681..74658572,2	Hela-S3	cervix:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC33-3	chr15:74648624-74648816	NONHSAT047227
2	lnc-CCDC33-3	chr15:74646867-74647026	NONHSAT047227
3	lnc-CCDC33-3	chr15:74643109-74643280	NONHSAT047227
4	lnc-CCDC33-3	chr15:74653893-74654382	NR_045207
5	lnc-CCDC33-3	chr15:74653855-74656961	NONHSAT047228
6	lnc-CCDC33-3	chr15:74653855-74654244	NONHSAT047227
7	lnc-CCDC33-3	chr15:74646797-74647026	NONHSAT047228

No data

Variant related genes	Relation type
ENSG00000261821	TF binding region
ENSG00000260266	TF binding region
CYP11A1	TF binding region
ENSG00000261821	CpG island
ENSG00000260266	CpG island
CYP11A1	CpG island
ENSG00000047410	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000150760	chromatin interactions
ENSG00000260266	chromatin interactions
ENSG00000070495	chromatin interactions
ENSG00000181038	chromatin interactions
ENSG00000200169	chromatin interactions

Extended variants
information (count: 588 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531523602	chr15:74640378-74640379	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552357528	chr15:74640381-74640382	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200935336	chr15:74640382-74640383	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190764523	chr15:74640386-74640387	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546976108	chr15:74640395-74640396	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374236209	chr15:74640405-74640406	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368916882	chr15:74640429-74640430	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145866066	chr15:74640446-74640447	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568472578	chr15:74640457-74640458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145527597	chr15:74640460-74640461	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113729254	chr15:74640469-74640470	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148872528	chr15:74640504-74640505	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539893175	chr15:74640522-74640523	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs6495096	chr15:74640647-74640648	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs373249464	chr15:74640674-74640675	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182585985	chr15:74640699-74640700	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114927930	chr15:74640750-74640751	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143558489	chr15:74640755-74640756	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs17515476	chr15:74640785-74640786	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574642883	chr15:74640815-74640816	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs78254926	chr15:74640816-74640817	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541483067	chr15:74640851-74640852	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563250026	chr15:74640856-74640857	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186644053	chr15:74640898-74640899	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545488151	chr15:74640969-74640970	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377504597	chr15:74640989-74640990	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370730401	chr15:74641000-74641001	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564388587	chr15:74641002-74641003	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372466454	chr15:74641020-74641021	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540953774	chr15:74641143-74641144	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77460826	chr15:74641192-74641193	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs60337947	chr15:74641233-74641234	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576579207	chr15:74641245-74641246	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562258004	chr15:74641391-74641392	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77678571	chr15:74641399-74641400	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58844886	chr15:74641410-74641411	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7175214	chr15:74641419-74641420	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs41553612	chr15:74641435-74641436	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs74335143	chr15:74641436-74641437	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12898858	chr15:74641464-74641465	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs148052823	chr15:74641482-74641483	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs534535355	chr15:74641532-74641533	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs546308028	chr15:74641576-74641577	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs553106253	chr15:74641596-74641597	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370638873	chr15:74641649-74641650	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs142675266	chr15:74641687-74641688	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs535701173	chr15:74641691-74641692	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375295866	chr15:74641736-74641737	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561309245	chr15:74641742-74641743	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs556582985	chr15:74641743-74641744	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74612000-74657800	Weak transcription	Right Atrium	heart
2	chr15:74628000-74642200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr15:74638000-74642800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr15:74638200-74642800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr15:74638600-74641400	Strong transcription	Placenta	Placenta
6	chr15:74640000-74640800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:74640600-74642200	Enhancers	Ovary	ovary
8	chr15:74640800-74647200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:74641400-74641800	Enhancers	GM12878-XiMat	blood
10	chr15:74641400-74643000	Weak transcription	Placenta	Placenta
11	chr15:74642200-74643400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr15:74642200-74653800	Weak transcription	Ovary	ovary
13	chr15:74642600-74643200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr15:74642800-74643200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr15:74642800-74644000	Enhancers	H9 Cell Line	embryonic stem cell
16	chr15:74642800-74644400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr15:74642800-74644400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr15:74643000-74643600	Enhancers	Placenta	Placenta
19	chr15:74643000-74644200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr15:74643000-74644400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr15:74643200-74643600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr15:74643200-74644200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr15:74643200-74644200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr15:74643400-74644200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr15:74643400-74644200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr15:74643400-74644400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr15:74643400-74645200	Enhancers	H1 Cell Line	embryonic stem cell
28	chr15:74643600-74643800	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr15:74643600-74644200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr15:74643600-74644200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr15:74643600-74644400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr15:74643600-74647200	Weak transcription	Placenta	Placenta
33	chr15:74643800-74644000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr15:74643800-74644200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:74643800-74644200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr15:74644000-74644400	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr15:74644200-74645200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr15:74644200-74650200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr15:74644200-74656800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:74644400-74645000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr15:74644400-74645600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr15:74644800-74646400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr15:74645000-74646000	Enhancers	Hela-S3	cervix
44	chr15:74645200-74646400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr15:74645600-74646200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr15:74646000-74649200	Weak transcription	Hela-S3	cervix
47	chr15:74646200-74650200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr15:74646400-74647200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr15:74646400-74647800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr15:74646800-74647400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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