Variant report

Variant	esv2760372
Chromosome Location	chr15:58721447-58731153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58722084-58722767	K562	blood:	n/a	n/a
2	ARID3A	chr15:58723845-58724674	HepG2	liver:	n/a	n/a
3	ATF1	chr15:58722141-58722665	K562	blood:	n/a	n/a
4	ATF3	chr15:58722156-58722424	K562	blood:	n/a	n/a
5	BHLHE40	chr15:58722117-58722772	K562	blood:	n/a	n/a
6	CBX3	chr15:58722012-58722972	K562	blood:	n/a	n/a
7	CBX3	chr15:58722094-58722498	K562	blood:	n/a	n/a
8	CCNT2	chr15:58722106-58722510	K562	blood:	n/a	n/a
9	CEBPB	chr15:58722209-58722479	K562	blood:	n/a	n/a
10	CEBPB	chr15:58724583-58724995	A549	lung:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
11	CEBPB	chr15:58724614-58724973	K562	blood:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
12	CEBPB	chr15:58724486-58725126	A549	lung:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
13	CEBPB	chr15:58723779-58724009	HepG2	liver:	n/a	chr15:58723909-58723921
14	CEBPB	chr15:58724526-58725075	Hela-S3	cervix:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
15	CEBPB	chr15:58724623-58725016	A549	lung:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
16	CEBPB	chr15:58724559-58725000	ECC-1	luminal epithelium:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
17	CEBPB	chr15:58724382-58724997	HepG2	liver:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
18	CEBPB	chr15:58724603-58724995	IMR90	lung:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
19	CEBPB	chr15:58724651-58724863	K562	blood:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
20	CEBPB	chr15:58724603-58724994	MCF-7	breast:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
21	CEBPB	chr15:58724543-58724992	ECC-1	luminal epithelium:	n/a	chr15:58724794-58724803 chr15:58724792-58724803 chr15:58724794-58724805 chr15:58724794-58724805 chr15:58724792-58724805 chr15:58724792-58724805 chr15:58724794-58724803 chr15:58724794-58724803 chr15:58724794-58724803
22	CEBPD	chr15:58722075-58722650	K562	blood:	n/a	n/a
23	CEBPD	chr15:58722106-58722612	K562	blood:	n/a	n/a
24	CHD2	chr15:58724546-58724991	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr15:58724597-58724629	K562	blood:	n/a	n/a
26	CHD2	chr15:58722219-58722419	K562	blood:	n/a	n/a
27	CTCF	chr15:58723560-58723710	Caco-2	colon:	n/a	n/a
28	CTCF	chr15:58726099-58726267	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:58726158-58726229	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:58731080-58731230	GM12864	blood:	n/a	n/a
31	CTCF	chr15:58726086-58726416	K562	blood:	n/a	n/a
32	CTCF	chr15:58731100-58731250	A549	lung:	n/a	n/a
33	CTCF	chr15:58726220-58726370	AG10803	skin:	n/a	n/a
34	CTCF	chr15:58730927-58731507	GM12878	blood:	n/a	n/a
35	CTCF	chr15:58722671-58722758	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr15:58731130-58731464	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr15:58731075-58731447	A549	lung:	n/a	n/a
38	CTCF	chr15:58730316-58731976	A549	lung:	n/a	chr15:58730772-58730785
39	CTCF	chr15:58726120-58726270	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr15:58722560-58722710	GM12864	blood:	n/a	n/a
41	CTCF	chr15:58722760-58722910	GM12866	blood:	n/a	n/a
42	CTCF	chr15:58722700-58722850	GM12865	blood:	n/a	n/a
43	CTCF	chr15:58722580-58722730	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr15:58726100-58726250	Caco-2	colon:	n/a	n/a
45	CTCF	chr15:58726140-58726290	BE2_C	brain:	n/a	n/a
46	CTCF	chr15:58722640-58722790	K562	blood:	n/a	n/a
47	CTCF	chr15:58725995-58726381	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:58722640-58722790	HepG2	liver:	n/a	n/a
49	CTCF	chr15:58726080-58726230	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr15:58726080-58726230	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58723879-58723929	T-47D	breast:	n/a
2	chr15:58723879-58723929	T-47D	breast:	n/a
3	chr15:58723851-58723901	GM12878	blood:	n/a
4	chr15:58723657-58723707	GM06990	blood:	n/a
5	chr15:58723657-58723707	HUVEC	blood vessel:	n/a
6	chr15:58723851-58723901	GM19239	blood:	n/a
7	chr15:58724041-58724091	NHBE	bronchial:	n/a
8	chr15:58724041-58724091	HRPEpiC	eye:	n/a
9	chr15:58724225-58724275	Caco-2	colon:	n/a
10	chr15:58724041-58724091	PANC-1	pancreas:	n/a
11	chr15:58723657-58723707	HAEpiC	amniotic membrane:	n/a
12	chr15:58723657-58723707	T-47D	breast:	n/a
13	chr15:58724041-58724091	GM06990	blood:	n/a
14	chr15:58723851-58723901	Hela-S3	cervix:	n/a
15	chr15:58724225-58724275	HCPEpiC	choroid plexus:	n/a
16	chr15:58723879-58723929	Hela-S3	cervix:	n/a
17	chr15:58724041-58724091	HRCEpiC	kidney:	n/a
18	chr15:58724041-58724091	PrEC	prostate:	n/a
19	chr15:58723879-58723929	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:58724225-58724275	IMR90	lung:	fetal
21	chr15:58723657-58723707	GM19239	blood:	n/a
22	chr15:58723851-58723901	NHDF-neo	bronchial:	n/a
23	chr15:58724225-58724275	AG09319	gingival:	n/a
24	chr15:58724041-58724091	MCF10A-Er-Src	breast:	n/a
25	chr15:58723657-58723707	K562	blood:	n/a
26	chr15:58723851-58723901	BE2_C	brain:	n/a
27	chr15:58723657-58723707	HIPEpiC	eye:	n/a
28	chr15:58724041-58724091	HEEpiC	esophagus:	n/a
29	chr15:58724225-58724275	A549	lung:	n/a
30	chr15:58723879-58723929	AG04449	skin:	fetal
31	chr15:58724041-58724091	AoSMC	blood vessel:	n/a
32	chr15:58723879-58723929	Hepatocyte	liver:	n/a
33	chr15:58724041-58724091	AG04450	lung:	fetal
34	chr15:58724225-58724275	HCT-116	colon:	n/a
35	chr15:58723657-58723707	AG10803	skin:	n/a
36	chr15:58723657-58723707	BJ	skin:	n/a
37	chr15:58724041-58724091	AG09309	skin:	n/a
38	chr15:58723879-58723929	HRE	kidney:	n/a
39	chr15:58723657-58723707	NH-A	brain:	n/a
40	chr15:58723879-58723929	HUVEC	blood vessel:	n/a
41	chr15:58723879-58723929	BE2_C	brain:	n/a
42	chr15:58723657-58723707	HCM	heart:	n/a
43	chr15:58723851-58723901	U87	brain:	n/a
44	chr15:58723851-58723901	ovcar-3	ovarian:	n/a
45	chr15:58723851-58723901	SAEC	small airway:	n/a
46	chr15:58724225-58724275	HRCEpiC	kidney:	n/a
47	chr15:58724225-58724275	AG04450	lung:	fetal
48	chr15:58724225-58724275	HL-60	blood:	n/a
49	chr15:58723851-58723901	MCF10A-Er-Src	breast:	n/a
50	chr15:58723851-58723901	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58623562..58626994-chr15:58730618..58733502,3	MCF-7	breast:
2	chr15:58730575..58732285-chr15:58839559..58842370,2	K562	blood:
3	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
4	chr15:58729567..58734283-chr15:58741092..58746394,5	K562	blood:
5	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
6	chr15:58714110..58717947-chr15:58718129..58721624,4	K562	blood:
7	chr15:58730817..58731598-chr22:22510997..22511880,2	HCT-116	colon:
8	chr15:58726222..58728488-chr15:58751000..58752953,2	K562	blood:
9	chr15:58709732..58712579-chr15:58730855..58732681,2	K562	blood:
10	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
11	chr15:58623609..58625282-chr15:58727962..58730632,2	MCF-7	breast:
12	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AQP9-5	chr15:58723026-58723350	NONHSAT044110
2	lnc-AQP9-5	chr15:58724192-58724562	NONHSAT044110
3	lnc-ALDH1A2-1	chr15:58727089-58729111	ENSG00000259293.1

Variant related genes	Relation type
LIPC	TF binding region
LIPC	CpG island
ENSG00000128918	chromatin interactions
ENSG00000233720	chromatin interactions

Extended variants
information (count: 465 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12912415	chr15:58721447-58721448	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548279706	chr15:58721512-58721513	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs141659461	chr15:58721515-58721516	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188060383	chr15:58721521-58721522	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565489246	chr15:58721581-58721582	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs113921288	chr15:58721584-58721585	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs369607007	chr15:58721595-58721596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs11071381	chr15:58721614-58721615	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530077878	chr15:58721647-58721648	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550044046	chr15:58721649-58721650	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs28687077	chr15:58721650-58721651	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs560481614	chr15:58721666-58721667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532443857	chr15:58721687-58721688	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139350107	chr15:58721688-58721689	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565563873	chr15:58721689-58721690	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs534393670	chr15:58721691-58721692	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs149022139	chr15:58721705-58721706	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs552085212	chr15:58721739-58721740	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs114304456	chr15:58721749-58721750	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs150597159	chr15:58721752-58721753	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs193014293	chr15:58721764-58721765	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556919997	chr15:58721785-58721786	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117082789	chr15:58721804-58721805	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28454089	chr15:58721813-58721814	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559173296	chr15:58721814-58721815	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572711688	chr15:58721822-58721823	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369957201	chr15:58721830-58721831	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs563221775	chr15:58721841-58721842	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs541526695	chr15:58721860-58721861	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561412984	chr15:58721871-58721872	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs530211685	chr15:58721890-58721891	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543409118	chr15:58721902-58721903	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200050110	chr15:58721948-58721949	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs139613628	chr15:58721952-58721953	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs582293	chr15:58721984-58721985	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532280457	chr15:58722007-58722008	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552083849	chr15:58722029-58722030	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565525202	chr15:58722046-58722047	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs1822830	chr15:58722047-58722048	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs11289628	chr15:58722074-58722075	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs528312251	chr15:58722080-58722081	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547879392	chr15:58722102-58722103	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568018652	chr15:58722119-58722120	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537160415	chr15:58722124-58722125	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550273686	chr15:58722134-58722135	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570456107	chr15:58722205-58722206	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs583662	chr15:58722276-58722277	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs559332656	chr15:58722283-58722284	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184505819	chr15:58722308-58722309	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs557247910	chr15:58722322-58722323	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58704600-58728800	Weak transcription	Thymus	Thymus
2	chr15:58711800-58722000	Enhancers	Liver	Liver
3	chr15:58716600-58721600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr15:58716600-58725800	Weak transcription	Right Atrium	heart
5	chr15:58716600-58726600	Weak transcription	Esophagus	oesophagus
6	chr15:58716800-58722400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:58717800-58723600	Weak transcription	Pancreas	Pancrea
8	chr15:58717800-58724400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:58718000-58724600	Weak transcription	NHDF-Ad	bronchial
10	chr15:58718200-58723600	Weak transcription	Fetal Intestine Large	intestine
11	chr15:58718400-58726600	Weak transcription	Stomach Mucosa	stomach
12	chr15:58718600-58725000	Weak transcription	Fetal Lung	lung
13	chr15:58718800-58723400	Weak transcription	A549	lung
14	chr15:58719600-58725800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:58720800-58723200	Weak transcription	HepG2	liver
16	chr15:58721200-58722000	Enhancers	K562	blood
17	chr15:58721600-58722000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr15:58721600-58722400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr15:58722000-58722600	Flanking Active TSS	K562	blood
20	chr15:58722000-58723800	Flanking Active TSS	Liver	Liver
21	chr15:58722000-58724400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr15:58722200-58722400	Enhancers	Fetal Thymus	thymus
23	chr15:58722200-58722600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:58722400-58722600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:58722400-58723600	Weak transcription	Fetal Thymus	thymus
26	chr15:58722600-58723800	Enhancers	K562	blood
27	chr15:58722600-58724200	Weak transcription	Right Ventricle	heart
28	chr15:58722600-58731000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr15:58723200-58723400	Enhancers	HepG2	liver
30	chr15:58723400-58724000	Flanking Active TSS	HepG2	liver
31	chr15:58723400-58724200	Enhancers	A549	lung
32	chr15:58723400-58724400	Enhancers	Fetal Kidney	kidney
33	chr15:58723600-58723800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr15:58723600-58724000	Enhancers	Pancreas	Pancrea
35	chr15:58723600-58724200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr15:58723600-58724200	Enhancers	Hela-S3	cervix
37	chr15:58723600-58724400	Enhancers	Fetal Thymus	thymus
38	chr15:58723600-58724600	Enhancers	Duodenum Mucosa	Duodenum
39	chr15:58723600-58725000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr15:58723600-58725000	Enhancers	Fetal Intestine Large	intestine
41	chr15:58723800-58724000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:58723800-58724000	Enhancers	Liver	Liver
43	chr15:58723800-58724400	Enhancers	Fetal Intestine Small	intestine
44	chr15:58723800-58724400	Weak transcription	K562	blood
45	chr15:58724000-58724400	Flanking Active TSS	Liver	Liver
46	chr15:58724000-58724400	Active TSS	HepG2	liver
47	chr15:58724000-58725800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:58724000-58725800	Weak transcription	Pancreas	Pancrea
49	chr15:58724200-58724400	Enhancers	Right Ventricle	heart
50	chr15:58724200-58724400	Flanking Active TSS	A549	lung

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