Variant report

Variant	esv18862
Chromosome Location	chr15:74642778-74659579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:611)
Chromatin interactive
region (count:5)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 50 per page) page: 1 2 3 4

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	chr15:74642801-74642924	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:74642703-74642956	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:74657579-74658706	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:74652339-74652875	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:74653307-74653601	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr15:74651954-74651980	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:74651813-74651942	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr15:74649871-74650178	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:74642726-74642926	K562	blood:	n/a	n/a
18	CHD1	chr15:74658179-74658186	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:74658087-74658199	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:74657259-74657450	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:74657405-74658677	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr15:74657673-74658494	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr15:74657793-74658431	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr15:74657790-74658743	HepG2	liver:	n/a	n/a
25	CREB1	chr15:74657699-74658750	HepG2	liver:	n/a	n/a
26	CTCF	chr15:74658080-74658230	SAEC	small airway:	n/a	n/a
27	CTCF	chr15:74658120-74658270	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr15:74658060-74658210	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr15:74658135-74658320	Fibrobl	skin:	n/a	n/a
30	CTCF	chr15:74658120-74658270	AG09319	gingival:	n/a	n/a
31	CTCF	chr15:74658120-74658270	GM06990	blood:	n/a	n/a
32	CTCF	chr15:74658196-74658302	GM19238	blood:	n/a	n/a
33	CTCF	chr15:74658140-74658290	HCM	heart:	n/a	n/a
34	CTCF	chr15:74658140-74658290	GM12871	blood:	n/a	n/a
35	CTCF	chr15:74658136-74658266	ProgFib	skin:	n/a	n/a
36	CTCF	chr15:74658340-74658490	AG04449	skin:	n/a	n/a
37	CTCF	chr15:74658120-74658270	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr15:74658122-74658306	HepG2	liver:	n/a	n/a
39	CTCF	chr15:74658140-74658290	AG04449	skin:	n/a	n/a
40	CTCF	chr15:74658215-74658283	GM13976	blood:	n/a	n/a
41	CTCF	chr15:74658060-74658210	BJ	skin:	n/a	n/a
42	CTCF	chr15:74645186-74645227	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr15:74658140-74658290	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr15:74658140-74658290	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr15:74658120-74658270	AG10803	skin:	n/a	n/a
46	CTCF	chr15:74658140-74658290	HAc	cerebellar:	n/a	n/a
47	CTCF	chr15:74658200-74658350	BJ	skin:	n/a	n/a
48	CTCF	chr15:74658100-74658250	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr15:74658100-74658250	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr15:74658140-74658290	NHDF-neo	bronchial:	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	chr15:74658330-74658380	AG10803	skin:	n/a
2	chr15:74658330-74658380	AG10803	skin:	n/a
3	chr15:74658573-74658623	HMEC	breast:	n/a
4	chr15:74658981-74659031	T-47D	breast:	n/a
5	chr15:74658981-74659031	SK-N-SH_RA	brain:	n/a
6	chr15:74658244-74658294	HMEC	breast:	n/a
7	chr15:74658981-74659031	SK-N-SH	brain:	n/a
8	chr15:74658330-74658380	MCF10A-Er-Src	breast:	n/a
9	chr15:74657911-74657961	Hepatocyte	liver:	n/a
10	chr15:74658653-74658703	Hela-S3	cervix:	n/a
11	chr15:74645873-74645923	K562	blood:	n/a
12	chr15:74657911-74657961	ProgFib	skin:	n/a
13	chr15:74645873-74645923	HMEC	breast:	n/a
14	chr15:74658330-74658380	BE2_C	brain:	n/a
15	chr15:74658547-74658597	H1-hESC	embryonic stem cell:	embryo
16	chr15:74658573-74658623	SAEC	small airway:	n/a
17	chr15:74657911-74657961	SK-N-SH_RA	brain:	n/a
18	chr15:74645873-74645923	MCF-7	breast:	n/a
19	chr15:74658573-74658623	ECC-1	luminal epithelium:	n/a
20	chr15:74645873-74645923	AG09309	skin:	n/a
21	chr15:74658547-74658597	HEK293	kidney:	embryo
22	chr15:74658547-74658597	AG09309	skin:	n/a
23	chr15:74658653-74658703	PFSK-1	brain:	n/a
24	chr15:74658553-74658603	SK-N-MC	brain:	n/a
25	chr15:74658547-74658597	AG09319	gingival:	n/a
26	chr15:74658166-74658216	T-47D	breast:	n/a
27	chr15:74658244-74658294	SK-N-MC	brain:	n/a
28	chr15:74658244-74658294	NH-A	brain:	n/a
29	chr15:74658573-74658623	HRPEpiC	eye:	n/a
30	chr15:74658573-74658623	AG09309	skin:	n/a
31	chr15:74658981-74659031	HCM	heart:	n/a
32	chr15:74658330-74658380	NT2-D1	testis:	n/a
33	chr15:74657911-74657961	GM12891	blood:	n/a
34	chr15:74658573-74658623	IMR90	lung:	fetal
35	chr15:74658573-74658623	HRCEpiC	kidney:	n/a
36	chr15:74658553-74658603	HCF	heart:	n/a
37	chr15:74658166-74658216	AG09319	gingival:	n/a
38	chr15:74658653-74658703	MCF-7	breast:	n/a
39	chr15:74658573-74658623	ProgFib	skin:	n/a
40	chr15:74658166-74658216	HAEpiC	amniotic membrane:	n/a
41	chr15:74658553-74658603	HNPCEpiC	eye:	n/a
42	chr15:74658553-74658603	BJ	skin:	n/a
43	chr15:74658166-74658216	HRCEpiC	kidney:	n/a
44	chr15:74658166-74658216	AG10803	skin:	n/a
45	chr15:74645873-74645923	Hela-S3	cervix:	n/a
46	chr15:74657911-74657961	HEEpiC	esophagus:	n/a
47	chr15:74658166-74658216	NHBE	bronchial:	n/a
48	chr15:74657911-74657961	NHBE	bronchial:	n/a
49	chr15:74658573-74658623	PANC-1	pancreas:	n/a
50	chr15:74658573-74658623	T-47D	breast:	n/a

(count:5 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 525 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376818343	chr15:74642796-74642797	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs115712429	chr15:74642834-74642835	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552160836	chr15:74642909-74642910	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs560480429	chr15:74642967-74642968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1843090	chr15:74643034-74643035	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs553450468	chr15:74643098-74643099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28671731	chr15:74643140-74643141	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs150637666	chr15:74643150-74643151	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs76824156	chr15:74643177-74643178	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs574194078	chr15:74643181-74643182	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs529072338	chr15:74643221-74643222	Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs550329474	chr15:74643308-74643309	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs139794652	chr15:74643319-74643320	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149396870	chr15:74643322-74643323	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs550968040	chr15:74643362-74643363	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs370023365	chr15:74643374-74643375	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs35153064	chr15:74643388-74643389	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs566451187	chr15:74643432-74643433	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs80128318	chr15:74643472-74643473	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs555417943	chr15:74643507-74643508	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs202136761	chr15:74643508-74643509	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs78100434	chr15:74643520-74643521	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs144789250	chr15:74643560-74643561	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs538456772	chr15:74643616-74643617	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1132670	chr15:74643665-74643666	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78261945	chr15:74643666-74643667	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140144836	chr15:74643671-74643672	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545707644	chr15:74643683-74643684	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560333931	chr15:74643684-74643685	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572385679	chr15:74643699-74643700	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542791799	chr15:74643704-74643705	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7181332	chr15:74643714-74643715	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376098361	chr15:74643745-74643746	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56840493	chr15:74643754-74643755	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187297477	chr15:74643775-74643776	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562299888	chr15:74643819-74643820	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576523655	chr15:74643849-74643850	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113099791	chr15:74643862-74643863	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192188267	chr15:74643870-74643871	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551258510	chr15:74643946-74643947	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566372266	chr15:74643990-74643991	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533766535	chr15:74644092-74644093	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs116349145	chr15:74644099-74644100	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs140274563	chr15:74644136-74644137	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs537900443	chr15:74644226-74644227	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs539242170	chr15:74644271-74644272	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558911551	chr15:74644275-74644276	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs118155655	chr15:74644292-74644293	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369087233	chr15:74644334-74644335	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs60499738	chr15:74644341-74644342	Enhancers Weak transcription Active TSS	n/a	n/a	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:447 , 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	chr15:74638000-74642800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr15:74638200-74642800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:74640800-74647200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:74641400-74643000	Weak transcription	Placenta	Placenta
6	chr15:74642200-74643400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr15:74642200-74653800	Weak transcription	Ovary	ovary
8	chr15:74642600-74643200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr15:74642800-74643200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr15:74642800-74644000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr15:74642800-74644400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr15:74642800-74644400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr15:74643000-74643600	Enhancers	Placenta	Placenta
14	chr15:74643000-74644200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr15:74643000-74644400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr15:74643200-74643600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr15:74643200-74644200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr15:74643200-74644200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr15:74643400-74644200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr15:74643400-74644200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr15:74643400-74644400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:74643400-74645200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr15:74643600-74643800	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr15:74643600-74644200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr15:74643600-74644200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:74643600-74644400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr15:74643600-74647200	Weak transcription	Placenta	Placenta
28	chr15:74643800-74644000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr15:74643800-74644200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:74643800-74644200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:74644000-74644400	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr15:74644200-74645200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr15:74644200-74650200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:74644200-74656800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:74644400-74645000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr15:74644400-74645600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr15:74644800-74646400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr15:74645000-74646000	Enhancers	Hela-S3	cervix
39	chr15:74645200-74646400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr15:74645600-74646200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr15:74646000-74649200	Weak transcription	Hela-S3	cervix
42	chr15:74646200-74650200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr15:74646400-74647200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr15:74646400-74647800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr15:74646800-74647400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr15:74647200-74647400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr15:74647200-74647400	Enhancers	Esophagus	oesophagus
48	chr15:74647200-74648000	Enhancers	Lung	lung
49	chr15:74647200-74648600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr15:74647200-74648800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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