Variant report

Variant	nsv597297
Chromosome Location	chr5:16174133-16180115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:915)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:16178853-16179248	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr5:16178898-16179206	K562	blood:	n/a	n/a
3	CHD1	chr5:16178992-16179348	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
4	CHD2	chr5:16178920-16179263	H1-hESC	embryonic stem cell:	n/a	chr5:16179097-16179107
5	CTBP2	chr5:16178961-16179519	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr5:16179176-16179184	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:16179292-16179401	Pancreas_OC	pancreas:	n/a	n/a
8	CTCF	chr5:16179300-16179450	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr5:16179016-16179460	MCF-7	breast:	n/a	chr5:16179111-16179124
10	CTCF	chr5:16178981-16179121	Fibrobl	skin:	n/a	n/a
11	CTCF	chr5:16179047-16179173	MCF-7	breast:	n/a	chr5:16179111-16179124
12	CTCF	chr5:16178980-16179130	SK-N-SH_RA	brain:	n/a	chr5:16179111-16179124
13	CTCF	chr5:16179010-16179444	MCF-7	breast:	n/a	chr5:16179111-16179124
14	CTCF	chr5:16179258-16179441	LNCaP	prostate:	n/a	n/a
15	CTCF	chr5:16179240-16179390	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr5:16179240-16179390	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr5:16179243-16179405	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:16179200-16179350	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr5:16179020-16179170	HBMEC	blood vessel:	n/a	chr5:16179111-16179124
20	CTCF	chr5:16179260-16179410	BE2_C	brain:	n/a	n/a
21	CTCF	chr5:16180080-16180230	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr5:16179200-16179350	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr5:16179032-16179108	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:16178992-16179431	MCF-7	breast:	n/a	chr5:16179111-16179124
25	CTCF	chr5:16178940-16179090	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr5:16179280-16179430	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:16179760-16179910	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr5:16179255-16179416	SK-N-SH_RA	brain:	n/a	n/a
29	E2F6	chr5:16180078-16180910	H1-hESC	embryonic stem cell:	n/a	chr5:16180114-16180124
30	EGR1	chr5:16178924-16179279	H1-hESC	embryonic stem cell:	n/a	n/a
31	EP300	chr5:16178862-16179409	H1-hESC	embryonic stem cell:	n/a	chr5:16178915-16178924
32	FOSL1	chr5:16178958-16179218	H1-hESC	embryonic stem cell:	n/a	n/a
33	FOXA1	chr5:16178974-16179183	T-47D	breast:	n/a	n/a
34	GABPA	chr5:16178922-16179438	H1-hESC	embryonic stem cell:	n/a	n/a
35	GATA3	chr5:16178936-16179278	T-47D	breast:	n/a	chr5:16178977-16178987
36	GATA3	chr5:16178988-16179323	MCF-7	breast:	n/a	n/a
37	GATA3	chr5:16178903-16179246	T-47D	breast:	n/a	chr5:16178977-16178987
38	GATA3	chr5:16174095-16174461	SH-SY5Y	brain:	n/a	chr5:16174156-16174172 chr5:16174153-16174174
39	GATA3	chr5:16175787-16176151	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr5:16177135-16177296	SH-SY5Y	brain:	n/a	n/a
41	HA-E2F1	chr5:16178836-16179359	MCF-7	breast:	n/a	n/a
42	HDAC2	chr5:16178902-16179432	MCF-7	breast:	n/a	chr5:16179067-16179086
43	HDAC2	chr5:16178909-16179270	MCF-7	breast:	n/a	chr5:16179067-16179086
44	HMGN3	chr5:16179054-16179215	K562	blood:	n/a	n/a
45	JUN	chr5:16178929-16179164	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr5:16178676-16179219	H1-hESC	embryonic stem cell:	n/a	chr5:16178697-16178707
47	MAFK	chr5:16177773-16177910	HepG2	liver:	n/a	n/a
48	MAX	chr5:16178826-16179406	MCF-7	breast:	n/a	n/a
49	MAX	chr5:16178882-16179405	ECC-1	luminal epithelium:	n/a	n/a
50	MAX	chr5:16178834-16179371	H1-hESC	embryonic stem cell:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16175867-16175917	HNPCEpiC	eye:	n/a
2	chr5:16180072-16180122	BE2_C	brain:	n/a
3	chr5:16179633-16179683	HMEC	breast:	n/a
4	chr5:16179210-16179260	Caco-2	colon:	n/a
5	chr5:16180062-16180112	SKMC	muscle:	n/a
6	chr5:16180033-16180083	GM12891	blood:	n/a
7	chr5:16180062-16180112	HMEC	breast:	n/a
8	chr5:16180076-16180126	SAEC	small airway:	n/a
9	chr5:16180048-16180098	HAEpiC	amniotic membrane:	n/a
10	chr5:16180076-16180126	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:16179633-16179683	GM12878	blood:	n/a
12	chr5:16179873-16179923	Caco-2	colon:	n/a
13	chr5:16180048-16180098	NT2-D1	testis:	n/a
14	chr5:16179135-16179185	HCT-116	colon:	n/a
15	chr5:16179135-16179185	HL-60	blood:	n/a
16	chr5:16175867-16175917	HIPEpiC	eye:	n/a
17	chr5:16180062-16180112	SK-N-SH_RA	brain:	n/a
18	chr5:16179210-16179260	MCF-7	breast:	n/a
19	chr5:16179135-16179185	IMR90	lung:	fetal
20	chr5:16179210-16179260	AG10803	skin:	n/a
21	chr5:16180072-16180122	Hepatocyte	liver:	n/a
22	chr5:16178784-16178834	NHDF-neo	bronchial:	n/a
23	chr5:16179012-16179062	GM06990	blood:	n/a
24	chr5:16179012-16179062	HNPCEpiC	eye:	n/a
25	chr5:16180062-16180112	T-47D	breast:	n/a
26	chr5:16179210-16179260	AG09309	skin:	n/a
27	chr5:16179012-16179062	HCT-116	colon:	n/a
28	chr5:16179873-16179923	HL-60	blood:	n/a
29	chr5:16179660-16179710	NHBE	bronchial:	n/a
30	chr5:16175867-16175917	HUVEC	blood vessel:	n/a
31	chr5:16180072-16180122	HCT-116	colon:	n/a
32	chr5:16178784-16178834	ECC-1	luminal epithelium:	n/a
33	chr5:16179135-16179185	K562	blood:	n/a
34	chr5:16175867-16175917	GM12891	blood:	n/a
35	chr5:16180033-16180083	ovcar-3	ovarian:	n/a
36	chr5:16180072-16180122	GM06990	blood:	n/a
37	chr5:16180062-16180112	GM12892	blood:	n/a
38	chr5:16179012-16179062	GM12891	blood:	n/a
39	chr5:16180062-16180112	AG09319	gingival:	n/a
40	chr5:16179135-16179185	AG09309	skin:	n/a
41	chr5:16179135-16179185	HCPEpiC	choroid plexus:	n/a
42	chr5:16180033-16180083	Jurkat	blood:	n/a
43	chr5:16179210-16179260	SAEC	small airway:	n/a
44	chr5:16178784-16178834	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:16175867-16175917	SK-N-SH	brain:	n/a
46	chr5:16180076-16180126	SK-N-SH_RA	brain:	n/a
47	chr5:16180068-16180118	A549	lung:	n/a
48	chr5:16180076-16180126	CMK	blood:	n/a
49	chr5:16179210-16179260	HIPEpiC	eye:	n/a
50	chr5:16180072-16180122	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:16177598..16179739-chr5:16465554..16467569,2	MCF-7	breast:
2	chr5:15898065..15900379-chr5:16172599..16174745,2	K562	blood:

No data

Variant related genes	Relation type
MARCH11	TF binding region
ENSG00000250448	TF binding region
MARCH11	CpG island
ENSG00000250448	CpG island
ENSG00000173545	chromatin interactions

Extended variants
information (count: 182 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:182 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538321626	chr5:16174141-16174142	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556125415	chr5:16174156-16174157	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147311824	chr5:16174175-16174176	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574353163	chr5:16174192-16174193	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572805638	chr5:16174210-16174211	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535753237	chr5:16174212-16174213	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554066535	chr5:16174237-16174238	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536826999	chr5:16174238-16174239	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572086234	chr5:16174317-16174318	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545787253	chr5:16174324-16174325	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189277949	chr5:16174346-16174347	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180872969	chr5:16174380-16174381	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576088276	chr5:16174392-16174393	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185747437	chr5:16174397-16174398	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576608364	chr5:16174399-16174400	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562985117	chr5:16174443-16174444	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530193279	chr5:16174461-16174462	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190064623	chr5:16174462-16174463	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183119035	chr5:16174558-16174559	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185968063	chr5:16174580-16174581	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148738101	chr5:16174630-16174631	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141487447	chr5:16174635-16174636	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs60041363	chr5:16174705-16174706	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs171058	chr5:16174723-16174724	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550203411	chr5:16174749-16174750	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370611335	chr5:16174752-16174753	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535610516	chr5:16174781-16174782	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376222048	chr5:16174801-16174802	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368261138	chr5:16174835-16174836	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114763220	chr5:16174846-16174847	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557506893	chr5:16174848-16174849	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575985174	chr5:16174857-16174858	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs163726	chr5:16174863-16174864	Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs342545	chr5:16174903-16174904	Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs139793313	chr5:16174981-16174982	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369842948	chr5:16175039-16175040	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542049295	chr5:16175071-16175072	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560301612	chr5:16175095-16175096	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528018013	chr5:16175105-16175106	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116407854	chr5:16175106-16175107	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541435822	chr5:16175108-16175109	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564327071	chr5:16175138-16175139	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs342546	chr5:16175139-16175140	Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550021758	chr5:16175160-16175161	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568512896	chr5:16175184-16175185	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529969711	chr5:16175248-16175249	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529383419	chr5:16175276-16175277	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547646361	chr5:16175358-16175359	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565868683	chr5:16175369-16175370	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139227878	chr5:16175375-16175376	Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16169400-16174600	Enhancers	Fetal Heart	heart
2	chr5:16171400-16176600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:16174600-16176000	Genic enhancers	Fetal Heart	heart
4	chr5:16175600-16175800	Enhancers	HMEC	breast
5	chr5:16176000-16177000	Enhancers	Fetal Heart	heart
6	chr5:16176600-16177200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:16177000-16177400	Flanking Active TSS	Fetal Heart	heart
8	chr5:16177200-16178400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:16177400-16177800	Enhancers	Fetal Heart	heart
10	chr5:16177800-16178200	Flanking Active TSS	Fetal Heart	heart
11	chr5:16178000-16179400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:16178200-16179000	Active TSS	Fetal Heart	heart
13	chr5:16178200-16179200	Active TSS	Brain Angular Gyrus	brain
14	chr5:16178200-16179400	Active TSS	Brain Anterior Caudate	brain
15	chr5:16178400-16179000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
16	chr5:16178400-16179400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:16178400-16179400	Active TSS	Brain Cingulate Gyrus	brain
18	chr5:16178400-16179400	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr5:16178600-16178800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:16178600-16178800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr5:16178600-16178800	Bivalent Enhancer	Fetal Brain Male	brain
22	chr5:16178600-16179000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
23	chr5:16178600-16179400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
24	chr5:16178600-16179600	Enhancers	Gastric	stomach
25	chr5:16178600-16180200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:16178600-16181000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
27	chr5:16178800-16179000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr5:16178800-16179000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:16178800-16179000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
31	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
32	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
33	chr5:16178800-16179000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
35	chr5:16178800-16179000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
36	chr5:16178800-16179000	Bivalent Enhancer	Fetal Intestine Small	intestine
37	chr5:16178800-16179000	Bivalent Enhancer	Ovary	ovary
38	chr5:16178800-16179000	Enhancers	Right Ventricle	heart
39	chr5:16178800-16179200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
40	chr5:16178800-16179400	Bivalent/Poised TSS	NH-A	brain
41	chr5:16178800-16179800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:16178800-16180600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
43	chr5:16179000-16179200	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:16179000-16179200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:16179000-16179200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:16179000-16179200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
47	chr5:16179000-16179200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr5:16179000-16179400	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr5:16179000-16179400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr5:16179000-16179400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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