Variant report

Variant	nsv904229
Chromosome Location	chr15:54267610-54340070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:263)
CpG islands
(count:550)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:54270443-54270603	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr15:54269100-54269383	GM12878	blood:	n/a	chr15:54269243-54269254
3	BHLHE40	chr15:54269170-54269333	HepG2	liver:	n/a	n/a
4	BHLHE40	chr15:54269065-54269371	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:54270556-54270727	GM12878	blood:	n/a	n/a
6	CEBPB	chr15:54327914-54328190	A549	lung:	n/a	chr15:54328041-54328052
7	CEBPB	chr15:54272984-54273248	HepG2	liver:	n/a	chr15:54273084-54273095
8	CEBPB	chr15:54327869-54328210	HepG2	liver:	n/a	chr15:54328041-54328052
9	CEBPB	chr15:54334058-54334298	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:54338360-54338559	A549	lung:	n/a	n/a
11	CEBPB	chr15:54335334-54335567	HepG2	liver:	n/a	chr15:54335407-54335420 chr15:54335407-54335420
12	CEBPB	chr15:54327868-54328211	Hela-S3	cervix:	n/a	chr15:54328041-54328052
13	CEBPB	chr15:54317233-54317453	IMR90	lung:	n/a	n/a
14	CHD1	chr15:54275962-54276044	GM12878	blood:	n/a	n/a
15	CHD1	chr15:54270369-54270604	GM12878	blood:	n/a	n/a
16	CHD1	chr15:54271429-54271624	GM12878	blood:	n/a	n/a
17	CHD2	chr15:54269281-54269328	HepG2	liver:	n/a	n/a
18	CHD2	chr15:54270395-54270817	GM12878	blood:	n/a	n/a
19	CTCF	chr15:54322960-54323110	MCF-7	breast:	n/a	n/a
20	CTCF	chr15:54269160-54269310	BE2_C	brain:	n/a	n/a
21	CTCF	chr15:54269120-54269270	Caco-2	colon:	n/a	n/a
22	CTCF	chr15:54268911-54269511	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:54269202-54269247	Gliobla	brain:	n/a	n/a
24	CTCF	chr15:54269188-54269272	GM12878	blood:	n/a	n/a
25	CTCF	chr15:54269140-54269290	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr15:54269146-54269262	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr15:54269220-54269370	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr15:54269200-54269350	A549	lung:	n/a	n/a
29	CTCF	chr15:54269100-54269250	RPTEC	kidney:	n/a	n/a
30	CTCF	chr15:54269100-54269250	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:54269188-54269243	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr15:54269140-54269290	HPF	lung:	n/a	n/a
33	CTCF	chr15:54269160-54269310	GM12878	blood:	n/a	n/a
34	CTCF	chr15:54269115-54269312	A549	lung:	n/a	n/a
35	CTCF	chr15:54270480-54270630	BE2_C	brain:	n/a	n/a
36	CTCF	chr15:54270300-54270450	HRE	kidney:	n/a	n/a
37	CTCF	chr15:54270466-54270655	MCF-7	breast:	n/a	n/a
38	CTCF	chr15:54269117-54269300	HepG2	liver:	n/a	n/a
39	CTCF	chr15:54270580-54270730	HMEC	breast:	n/a	n/a
40	CTCF	chr15:54269160-54269310	HepG2	liver:	n/a	n/a
41	CTCF	chr15:54269109-54269337	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:54269120-54269270	HEK293	kidney:	n/a	n/a
43	CTCF	chr15:54269120-54269270	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr15:54269088-54269322	HepG2	liver:	n/a	n/a
45	CTCF	chr15:54269120-54269270	HPF	lung:	n/a	n/a
46	CTCF	chr15:54269117-54269349	A549	lung:	n/a	n/a
47	CTCF	chr15:54269180-54269330	RPTEC	kidney:	n/a	n/a
48	CTCF	chr15:54269140-54269290	GM12869	blood:	n/a	n/a
49	CTCF	chr15:54269200-54269350	GM06990	blood:	n/a	n/a
50	CTCF	chr15:54270420-54270570	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54270557-54270607	HRCEpiC	kidney:	n/a
2	chr15:54270557-54270607	HRCEpiC	kidney:	n/a
3	chr15:54303927-54303977	LNCaP	prostate:	n/a
4	chr15:54271167-54271217	IMR90	lung:	fetal
5	chr15:54270947-54270997	SAEC	small airway:	n/a
6	chr15:54270693-54270743	HEEpiC	esophagus:	n/a
7	chr15:54304950-54305000	SK-N-SH_RA	brain:	n/a
8	chr15:54270693-54270743	HEK293	kidney:	embryo
9	chr15:54271167-54271217	HNPCEpiC	eye:	n/a
10	chr15:54270557-54270607	T-47D	breast:	n/a
11	chr15:54304950-54305000	PFSK-1	brain:	n/a
12	chr15:54270947-54270997	GM12892	blood:	n/a
13	chr15:54304778-54304828	HUVEC	blood vessel:	n/a
14	chr15:54270557-54270607	SK-N-SH_RA	brain:	n/a
15	chr15:54270661-54270711	IMR90	lung:	fetal
16	chr15:54270557-54270607	HCM	heart:	n/a
17	chr15:54270947-54270997	Jurkat	blood:	n/a
18	chr15:54305206-54305256	HNPCEpiC	eye:	n/a
19	chr15:54270693-54270743	HAEpiC	amniotic membrane:	n/a
20	chr15:54270557-54270607	K562	blood:	n/a
21	chr15:54304950-54305000	LNCaP	prostate:	n/a
22	chr15:54305206-54305256	HPAEpiC	pulmonary alveolar:	n/a
23	chr15:54304950-54305000	SK-N-MC	brain:	n/a
24	chr15:54304778-54304828	AG09319	gingival:	n/a
25	chr15:54270557-54270607	SK-N-MC	brain:	n/a
26	chr15:54271167-54271217	AG09319	gingival:	n/a
27	chr15:54270947-54270997	U87	brain:	n/a
28	chr15:54270947-54270997	HRPEpiC	eye:	n/a
29	chr15:54270947-54270997	HRCEpiC	kidney:	n/a
30	chr15:54270557-54270607	AG04450	lung:	fetal
31	chr15:54304950-54305000	HRPEpiC	eye:	n/a
32	chr15:54305206-54305256	K562	blood:	n/a
33	chr15:54270557-54270607	HEEpiC	esophagus:	n/a
34	chr15:54270693-54270743	Hepatocyte	liver:	n/a
35	chr15:54303927-54303977	NH-A	brain:	n/a
36	chr15:54270557-54270607	AG09309	skin:	n/a
37	chr15:54304950-54305000	HUVEC	blood vessel:	n/a
38	chr15:54304778-54304828	NHDF-neo	bronchial:	n/a
39	chr15:54304950-54305000	GM12878	blood:	n/a
40	chr15:54270661-54270711	NHDF-neo	bronchial:	n/a
41	chr15:54303927-54303977	NHDF-neo	bronchial:	n/a
42	chr15:54270693-54270743	NH-A	brain:	n/a
43	chr15:54270947-54270997	PANC-1	pancreas:	n/a
44	chr15:54270693-54270743	PrEC	prostate:	n/a
45	chr15:54270693-54270743	HCT-116	colon:	n/a
46	chr15:54270693-54270743	HepG2	liver:	n/a
47	chr15:54270557-54270607	IMR90	lung:	fetal
48	chr15:54303927-54303977	SKMC	muscle:	n/a
49	chr15:54304950-54305000	K562	blood:	n/a
50	chr15:54304950-54305000	Caco-2	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54266407..54270072-chr15:55486535..55491034,4	MCF-7	breast:
2	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
3	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
4	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
5	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
6	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
7	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
8	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
9	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
10	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
11	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
12	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
13	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-1	chr15:54268965-54269105	ENSG00000259669.1

No data

Variant related genes	Relation type
UNC13C	TF binding region
ENSG00000259669	TF binding region
UNC13C	CpG island
ENSG00000259669	CpG island
ENSG00000137876	chromatin interactions

Extended variants
information (count: 2839 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2839 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16973921	chr15:54267610-54267611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548937646	chr15:54267656-54267657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562380016	chr15:54267658-54267659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531090736	chr15:54267699-54267700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147895566	chr15:54267700-54267701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569700411	chr15:54267792-54267793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185690728	chr15:54267843-54267844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551735362	chr15:54267860-54267861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75603982	chr15:54267890-54267891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2725585	chr15:54268002-54268003	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554394766	chr15:54268071-54268072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532689508	chr15:54268072-54268073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574665473	chr15:54268089-54268090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79089277	chr15:54268091-54268092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34608053	chr15:54268130-54268131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs16973923	chr15:54268135-54268136	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546364342	chr15:54268165-54268166	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559772630	chr15:54268194-54268195	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368842496	chr15:54268222-54268223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573236557	chr15:54268223-54268224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542249911	chr15:54268257-54268258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562381119	chr15:54268273-54268274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369688074	chr15:54268276-54268277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs8024617	chr15:54268306-54268307	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs375829352	chr15:54268328-54268329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550582294	chr15:54268337-54268338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551138667	chr15:54268351-54268352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368693222	chr15:54268360-54268361	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564552826	chr15:54268399-54268400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188982058	chr15:54268448-54268449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551894357	chr15:54268489-54268490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565440122	chr15:54268516-54268517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536361110	chr15:54268564-54268565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2725586	chr15:54268576-54268577	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs547798511	chr15:54268603-54268604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199931417	chr15:54268639-54268640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568327749	chr15:54268640-54268641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373631619	chr15:54268646-54268647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201004679	chr15:54268653-54268654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs8030160	chr15:54268654-54268655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs199687244	chr15:54268655-54268656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs386784101	chr15:54268656-54268657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148861102	chr15:54268668-54268669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58720259	chr15:54268674-54268675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555071702	chr15:54268675-54268676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs10682648	chr15:54268683-54268684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs397937135	chr15:54268692-54268693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577003592	chr15:54268703-54268704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143633038	chr15:54268726-54268727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181748458	chr15:54268730-54268731	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	21509527	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54267400-54269600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:54269200-54269400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr15:54269200-54269400	Enhancers	Esophagus	oesophagus
4	chr15:54269200-54269400	Enhancers	Fetal Intestine Small	intestine
5	chr15:54269200-54270000	Enhancers	Fetal Brain Female	brain
6	chr15:54269200-54270000	Enhancers	Fetal Lung	lung
7	chr15:54269200-54277200	Active TSS	Aorta	Aorta
8	chr15:54269400-54270400	Weak transcription	Esophagus	oesophagus
9	chr15:54269600-54269800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr15:54269800-54270000	Bivalent Enhancer	Brain Hippocampus Middle	brain
11	chr15:54269800-54274800	Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr15:54270000-54270200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr15:54270000-54270200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:54270000-54270200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
15	chr15:54270000-54270200	Enhancers	Brain Germinal Matrix	brain
16	chr15:54270000-54270200	Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr15:54270000-54270200	Active TSS	Fetal Brain Male	brain
18	chr15:54270000-54270400	Flanking Active TSS	Fetal Brain Female	brain
19	chr15:54270000-54270600	Flanking Active TSS	Fetal Lung	lung
20	chr15:54270000-54270800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
21	chr15:54270000-54271600	Active TSS	Stomach Smooth Muscle	stomach
22	chr15:54270200-54270400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr15:54270200-54270400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:54270200-54270400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
26	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
27	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
28	chr15:54270200-54270400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr15:54270200-54270400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr15:54270200-54270400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr15:54270200-54270400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:54270200-54270400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr15:54270200-54270400	Active TSS	Fetal Intestine Small	intestine
34	chr15:54270200-54270400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
35	chr15:54270200-54270400	Active TSS	Fetal Muscle Leg	muscle
36	chr15:54270200-54270400	Enhancers	Gastric	stomach
37	chr15:54270200-54270400	Enhancers	Ovary	ovary
38	chr15:54270200-54270400	Enhancers	Pancreas	Pancrea
39	chr15:54270200-54270400	Enhancers	Placenta Amnion	Placenta Amnion
40	chr15:54270200-54270400	Active TSS	Rectal Smooth Muscle	rectum
41	chr15:54270200-54270400	Active TSS	A549	lung
42	chr15:54270200-54270600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:54270200-54270600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr15:54270200-54270600	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr15:54270200-54270600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
46	chr15:54270200-54270600	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr15:54270200-54270600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr15:54270200-54270600	Flanking Active TSS	Fetal Brain Male	brain
49	chr15:54270200-54270800	Active TSS	Brain Substantia Nigra	brain
50	chr15:54270200-54270800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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