Variant report

Variant	esv3510860
Chromosome Location	chr15:72898800-72949834
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr15:72929199-72929370	HepG2	liver:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
2	ATF3	chr15:72929209-72929423	K562	blood:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
3	ATF3	chr15:72929193-72929453	GM12878	blood:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
4	ATF3	chr15:72929169-72929468	H1-hESC	embryonic stem cell:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
5	BATF	chr15:72919770-72920027	GM12878	blood:	n/a	n/a
6	BATF	chr15:72925333-72925511	GM12878	blood:	n/a	n/a
7	BATF	chr15:72919762-72919946	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:72946954-72947101	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:72919704-72919991	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:72929114-72929321	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:72908161-72908487	HepG2	liver:	n/a	n/a
12	BHLHE40	chr15:72908169-72908359	K562	blood:	n/a	n/a
13	BHLHE40	chr15:72929099-72929473	HepG2	liver:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
14	BHLHE40	chr15:72929272-72929472	HepG2	liver:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
15	BHLHE40	chr15:72929274-72929469	K562	blood:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
16	CBX3	chr15:72928995-72929709	K562	blood:	n/a	n/a
17	CBX3	chr15:72929167-72929610	K562	blood:	n/a	n/a
18	CEBPB	chr15:72915707-72915783	K562	blood:	n/a	n/a
19	CEBPB	chr15:72929283-72929294	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr15:72915523-72915714	HepG2	liver:	n/a	chr15:72915625-72915636
21	CHD2	chr15:72929269-72929481	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr15:72929278-72929474	GM12878	blood:	n/a	n/a
23	CHD2	chr15:72929272-72929475	HepG2	liver:	n/a	n/a
24	CHD2	chr15:72929278-72929469	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:72908400-72908469	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr15:72929281-72929477	K562	blood:	n/a	n/a
27	CTCF	chr15:72920760-72920910	GM12869	blood:	n/a	n/a
28	CTCF	chr15:72920689-72920850	GM10266	blood:	n/a	n/a
29	CTCF	chr15:72907970-72908012	GM13976	blood:	n/a	n/a
30	CTCF	chr15:72920680-72920830	Caco-2	colon:	n/a	n/a
31	CTCF	chr15:72920671-72920830	A549	lung:	n/a	n/a
32	CTCF	chr15:72920780-72920930	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr15:72903507-72903899	A549	lung:	n/a	n/a
34	CTCF	chr15:72920680-72920830	AG09319	gingival:	n/a	n/a
35	CTCF	chr15:72903675-72903733	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr15:72920660-72920810	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr15:72920720-72920870	GM12878	blood:	n/a	n/a
38	CTCF	chr15:72920740-72920890	SAEC	small airway:	n/a	n/a
39	CTCF	chr15:72920700-72920850	AG09319	gingival:	n/a	n/a
40	CTCF	chr15:72920700-72920850	GM12868	blood:	n/a	n/a
41	CTCF	chr15:72908380-72908530	GM12870	blood:	n/a	n/a
42	CTCF	chr15:72920700-72920850	HMF	breast:	n/a	n/a
43	CTCF	chr15:72920646-72920859	GM12892	blood:	n/a	n/a
44	CTCF	chr15:72920517-72921005	K562	blood:	n/a	n/a
45	CTCF	chr15:72920681-72920797	Fibrobl	skin:	n/a	n/a
46	CTCF	chr15:72920740-72920890	HL-60	blood:	n/a	n/a
47	CTCF	chr15:72920680-72920830	HRE	kidney:	n/a	n/a
48	CTCF	chr15:72920518-72920917	K562	blood:	n/a	n/a
49	CTCF	chr15:72920680-72920830	GM12872	blood:	n/a	n/a
50	CTCF	chr15:72920720-72920870	HUVEC	blood vessel:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72929414-72929464	NH-A	brain:	n/a
2	chr15:72929414-72929464	NH-A	brain:	n/a
3	chr15:72929414-72929464	MCF10A-Er-Src	breast:	n/a
4	chr15:72929414-72929464	NT2-D1	testis:	n/a
5	chr15:72929414-72929464	HepG2	liver:	n/a
6	chr15:72929414-72929464	HCF	heart:	n/a
7	chr15:72929414-72929464	PrEC	prostate:	n/a
8	chr15:72929414-72929464	HMEC	breast:	n/a
9	chr15:72929414-72929464	H1-hESC	embryonic stem cell:	embryo
10	chr15:72929414-72929464	PANC-1	pancreas:	n/a
11	chr15:72929414-72929464	HRE	kidney:	n/a
12	chr15:72929414-72929464	SK-N-SH	brain:	n/a
13	chr15:72929414-72929464	MCF-7	breast:	n/a
14	chr15:72929414-72929464	NHDF-neo	bronchial:	n/a
15	chr15:72929414-72929464	SKMC	muscle:	n/a
16	chr15:72929414-72929464	AoSMC	blood vessel:	n/a
17	chr15:72929414-72929464	CMK	blood:	n/a
18	chr15:72929414-72929464	BE2_C	brain:	n/a
19	chr15:72929414-72929464	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:72929414-72929464	A549	lung:	n/a
21	chr15:72929414-72929464	HCM	heart:	n/a
22	chr15:72929414-72929464	GM12891	blood:	n/a
23	chr15:72929414-72929464	IMR90	lung:	fetal
24	chr15:72929414-72929464	HEEpiC	esophagus:	n/a
25	chr15:72929414-72929464	PFSK-1	brain:	n/a
26	chr15:72929414-72929464	RPTEC	kidney:	n/a
27	chr15:72929414-72929464	GM06990	blood:	n/a
28	chr15:72929414-72929464	ovcar-3	ovarian:	n/a
29	chr15:72929414-72929464	AG09319	gingival:	n/a
30	chr15:72929414-72929464	T-47D	breast:	n/a
31	chr15:72929414-72929464	NHBE	bronchial:	n/a
32	chr15:72929414-72929464	Jurkat	blood:	n/a
33	chr15:72929414-72929464	LNCaP	prostate:	n/a
34	chr15:72929414-72929464	GM12878	blood:	n/a
35	chr15:72929414-72929464	AG09309	skin:	n/a
36	chr15:72929414-72929464	HRPEpiC	eye:	n/a
37	chr15:72929414-72929464	HNPCEpiC	eye:	n/a
38	chr15:72929414-72929464	HUVEC	blood vessel:	n/a
39	chr15:72929414-72929464	HAEpiC	amniotic membrane:	n/a
40	chr15:72929414-72929464	GM19239	blood:	n/a
41	chr15:72929414-72929464	BJ	skin:	n/a
42	chr15:72929414-72929464	AG10803	skin:	n/a
43	chr15:72929414-72929464	GM12892	blood:	n/a
44	chr15:72929414-72929464	NB4	blood:	n/a
45	chr15:72929414-72929464	K562	blood:	n/a
46	chr15:72929414-72929464	HRCEpiC	kidney:	n/a
47	chr15:72929414-72929464	SK-N-MC	brain:	n/a
48	chr15:72929414-72929464	HCPEpiC	choroid plexus:	n/a
49	chr15:72929414-72929464	Caco-2	colon:	n/a
50	chr15:72929414-72929464	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:72766090..72768809-chr15:72908354..72909983,2	MCF-7	breast:
2	chr15:72916000..72918571-chr15:72920534..72922418,2	MCF-7	breast:
3	chr15:72902749..72904862-chr15:72907077..72909807,2	K562	blood:
4	chr15:72916000..72918571-chr15:72920534..72922418,2	MCF-7	breast:
5	chr15:72604977..72605618-chr15:72908296..72908821,2	K562	blood:
6	chr15:72902749..72904862-chr15:72907077..72909807,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARIH1-2	chr15:72908151-72910591	ENSG00000260672.1
2	lnc-HIGD2B-1	chr15:72929127-72929229	ENSG00000259783.1
3	lnc-HIGD2B-1	chr15:72900978-72901094	ENSG00000259783.1
4	lnc-HIGD2B-1	chr15:72925679-72925747	ENSG00000259783.1
5	lnc-HIGD2B-1	chr15:72908471-72908588	ENSG00000259783.1
6	lnc-GOLGA6B-1	chr15:72917445-72918348	NONHSAT047113
7	lnc-ARIH1-4	chr15:72904161-72904401	NONHSAT047111
8	lnc-HIGD2B-1	chr15:72900828-72901094	ENSG00000259783.1
9	lnc-HIGD2B-1	chr15:72929127-72929260	ENSG00000259783.1
10	lnc-HIGD2B-1	chr15:72925679-72925747	ENSG00000259783.1
11	lnc-GOLGA6B-1	chr15:72918523-72919351	NONHSAT047113

No data

Variant related genes	Relation type
ENSG00000259783	TF binding region
GOLGA6B	TF binding region
ENSG00000259909	TF binding region
RN7SL485P	TF binding region
ENSG00000260672	TF binding region
ENSG00000259783	CpG island
GOLGA6B	CpG island
ENSG00000259909	CpG island
RN7SL485P	CpG island
ENSG00000260672	CpG island
ENSG00000260672	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000243790	chromatin interactions

Extended variants
information (count: 1017 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1017 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112525607	chr15:72898844-72898845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74501840	chr15:72898914-72898915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549126229	chr15:72898915-72898916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567952452	chr15:72898949-72898950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538129227	chr15:72898994-72898995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550585001	chr15:72899005-72899006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4777521	chr15:72899025-72899026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188497434	chr15:72899157-72899158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141168402	chr15:72899200-72899201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572933490	chr15:72899224-72899225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533977531	chr15:72899229-72899230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372130615	chr15:72899324-72899325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192006419	chr15:72899337-72899338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544598115	chr15:72899350-72899351	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374632876	chr15:72899356-72899357	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544165563	chr15:72899357-72899358	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562932199	chr15:72899362-72899363	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs368153883	chr15:72899364-72899365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372156687	chr15:72899365-72899366	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374842286	chr15:72899370-72899371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368803757	chr15:72899371-72899372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564880387	chr15:72899374-72899375	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs374964861	chr15:72899375-72899376	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368863108	chr15:72899378-72899379	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs377246447	chr15:72899413-72899414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148173838	chr15:72899443-72899444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545140272	chr15:72899444-72899445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142019233	chr15:72899451-72899452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183273685	chr15:72899502-72899503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7497390	chr15:72899534-72899535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561307959	chr15:72899544-72899545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7497433	chr15:72899545-72899546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs554582934	chr15:72899594-72899595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187801824	chr15:72899646-72899647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568873479	chr15:72899648-72899649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539447554	chr15:72899655-72899656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191553187	chr15:72899664-72899665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549482878	chr15:72899683-72899684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34146373	chr15:72899685-72899686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569237078	chr15:72899699-72899700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111981852	chr15:72899743-72899744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62015889	chr15:72899748-72899749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200263100	chr15:72899771-72899772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373259745	chr15:72899778-72899779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60853325	chr15:72899791-72899792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142142515	chr15:72899803-72899804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538188285	chr15:72899842-72899843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556176565	chr15:72899848-72899849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28435710	chr15:72899991-72899992	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs28695207	chr15:72900028-72900029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	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
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72841000-72909000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:72870800-72902200	Weak transcription	Gastric	stomach
3	chr15:72874800-72899800	Weak transcription	Fetal Stomach	stomach
4	chr15:72876200-72903400	Weak transcription	Brain Germinal Matrix	brain
5	chr15:72876200-72907800	Weak transcription	Brain Substantia Nigra	brain
6	chr15:72876400-72903800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:72876800-72907600	Weak transcription	Lung	lung
8	chr15:72877800-72910000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:72878400-72907800	Weak transcription	Left Ventricle	heart
10	chr15:72879800-72906400	Weak transcription	Adipose Nuclei	Adipose
11	chr15:72883200-72909000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr15:72888000-72908200	Weak transcription	Right Ventricle	heart
13	chr15:72892600-72903600	Weak transcription	Brain Hippocampus Middle	brain
14	chr15:72894200-72899600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:72894600-72909000	Weak transcription	HSMMtube	muscle
16	chr15:72894800-72903800	Weak transcription	Fetal Intestine Small	intestine
17	chr15:72895200-72906000	Weak transcription	Fetal Brain Female	brain
18	chr15:72897600-72898800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:72898000-72898800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:72898000-72902000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr15:72898400-72906200	Weak transcription	Spleen	Spleen
22	chr15:72898400-72910600	Weak transcription	Esophagus	oesophagus
23	chr15:72898800-72899000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr15:72898800-72899000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:72899000-72902000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:72899200-72907600	Weak transcription	Right Atrium	heart
27	chr15:72899600-72899800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr15:72899800-72900600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:72899800-72900600	Enhancers	Fetal Stomach	stomach
30	chr15:72899800-72901200	Enhancers	HepG2	liver
31	chr15:72899800-72905600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr15:72899800-72908000	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr15:72900400-72908400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:72900600-72901200	Weak transcription	Fetal Stomach	stomach
35	chr15:72901200-72901400	Enhancers	Fetal Stomach	stomach
36	chr15:72902000-72902200	Enhancers	Pancreas	Pancrea
37	chr15:72902000-72902600	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr15:72902000-72902800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:72902200-72902400	Enhancers	Gastric	stomach
40	chr15:72902200-72907800	Weak transcription	Pancreas	Pancrea
41	chr15:72902600-72908400	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr15:72902800-72907000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:72904600-72904800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:72904600-72904800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:72904800-72905400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr15:72907000-72907400	Enhancers	H9 Cell Line	embryonic stem cell
47	chr15:72907000-72907800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:72907000-72909400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr15:72907000-72909400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr15:72907200-72907800	Enhancers	HUES64 Cell Line	embryonic stem cell

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