Variant report

Variant	nsv881357
Chromosome Location	chr5:30226419-30371238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:30279383-30279506	K562	blood:	n/a	n/a
2	ATF1	chr5:30334740-30334775	K562	blood:	n/a	n/a
3	BHLHE40	chr5:30337300-30337674	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:30337301-30337609	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:30274414-30274524	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr5:30274323-30274621	A549	lung:	n/a	chr5:30274549-30274560 chr5:30274549-30274560
7	CEBPB	chr5:30324366-30324430	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:30356521-30356732	A549	lung:	n/a	chr5:30356586-30356597
9	CEBPB	chr5:30274231-30274650	Hela-S3	cervix:	n/a	chr5:30274549-30274560 chr5:30274549-30274560
10	CEBPB	chr5:30326792-30327081	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:30274315-30274636	HepG2	liver:	n/a	chr5:30274549-30274560 chr5:30274549-30274560
12	CEBPB	chr5:30272424-30273185	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:30240967-30241039	HepG2	liver:	n/a	chr5:30240982-30240993
14	CEBPB	chr5:30336225-30336401	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:30284429-30284679	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:30284431-30284705	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:30356493-30356736	HepG2	liver:	n/a	chr5:30356586-30356597
18	CEBPB	chr5:30326920-30327209	MCF-7	breast:	n/a	n/a
19	CHD1	chr5:30239915-30239986	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr5:30239924-30240069	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr5:30272825-30273325	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr5:30324280-30324473	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:30324297-30324483	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:30324294-30324467	MCF-7	breast:	n/a	n/a
25	CTCF	chr5:30231419-30231492	GM10248	blood:	n/a	n/a
26	CTCF	chr5:30324203-30324488	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:30324274-30324491	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:30324320-30324470	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:30324200-30324350	A549	lung:	n/a	n/a
30	CTCF	chr5:30309360-30309510	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr5:30324343-30324406	LNCaP	prostate:	n/a	n/a
32	CTCF	chr5:30324320-30324470	BE2_C	brain:	n/a	n/a
33	CTCF	chr5:30366100-30366250	SAEC	small airway:	n/a	n/a
34	CTCF	chr5:30324140-30324430	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:30226740-30226890	GM12869	blood:	n/a	n/a
36	CTCF	chr5:30324320-30324470	RPTEC	kidney:	n/a	n/a
37	CTCF	chr5:30324374-30324398	HepG2	liver:	n/a	n/a
38	CTCF	chr5:30324280-30324430	Caco-2	colon:	n/a	n/a
39	CTCF	chr5:30324280-30324430	HEK293	kidney:	n/a	n/a
40	CTCF	chr5:30324260-30324410	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr5:30324340-30324490	K562	blood:	n/a	n/a
42	CTCF	chr5:30324267-30324486	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:30360680-30360830	K562	blood:	n/a	n/a
44	CTCF	chr5:30247596-30247636	ProgFib	skin:	n/a	n/a
45	CTCF	chr5:30324400-30324550	HepG2	liver:	n/a	n/a
46	CTCF	chr5:30321640-30321790	WI-38	lung:	n/a	n/a
47	CTCF	chr5:30299480-30299630	GM06990	blood:	n/a	n/a
48	CTCF	chr5:30324330-30324445	A549	lung:	n/a	n/a
49	CTCF	chr5:30361072-30361110	Lung_OC	lung:	n/a	n/a
50	CTCF	chr5:30324300-30324450	HCPEpiC	choroid plexus:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:30346164-30346214	ovcar-3	ovarian:	n/a
2	chr5:30346164-30346214	ovcar-3	ovarian:	n/a
3	chr5:30346020-30346070	GM12891	blood:	n/a
4	chr5:30346020-30346070	ovcar-3	ovarian:	n/a
5	chr5:30346164-30346214	NHBE	bronchial:	n/a
6	chr5:30346809-30346859	GM12891	blood:	n/a
7	chr5:30346164-30346214	AG04449	skin:	fetal
8	chr5:30346809-30346859	ProgFib	skin:	n/a
9	chr5:30346020-30346070	NHBE	bronchial:	n/a
10	chr5:30346164-30346214	Hepatocyte	liver:	n/a
11	chr5:30346809-30346859	IMR90	lung:	fetal
12	chr5:30346020-30346070	NH-A	brain:	n/a
13	chr5:30346020-30346070	AoSMC	blood vessel:	n/a
14	chr5:30346164-30346214	AoSMC	blood vessel:	n/a
15	chr5:30346164-30346214	U87	brain:	n/a
16	chr5:30346164-30346214	HRCEpiC	kidney:	n/a
17	chr5:30346809-30346859	HAEpiC	amniotic membrane:	n/a
18	chr5:30346020-30346070	HNPCEpiC	eye:	n/a
19	chr5:30346020-30346070	CMK	blood:	n/a
20	chr5:30346020-30346070	NB4	blood:	n/a
21	chr5:30346809-30346859	BE2_C	brain:	n/a
22	chr5:30346809-30346859	HCF	heart:	n/a
23	chr5:30346164-30346214	AG04450	lung:	fetal
24	chr5:30346020-30346070	AG04450	lung:	fetal
25	chr5:30346020-30346070	AG10803	skin:	n/a
26	chr5:30346809-30346859	GM06990	blood:	n/a
27	chr5:30346164-30346214	HL-60	blood:	n/a
28	chr5:30346164-30346214	HEEpiC	esophagus:	n/a
29	chr5:30346809-30346859	HEEpiC	esophagus:	n/a
30	chr5:30346809-30346859	HCPEpiC	choroid plexus:	n/a
31	chr5:30346020-30346070	HEK293	kidney:	embryo
32	chr5:30346809-30346859	Hepatocyte	liver:	n/a
33	chr5:30346809-30346859	SAEC	small airway:	n/a
34	chr5:30346809-30346859	HMEC	breast:	n/a
35	chr5:30346164-30346214	NB4	blood:	n/a
36	chr5:30346164-30346214	LNCaP	prostate:	n/a
37	chr5:30346020-30346070	HMEC	breast:	n/a
38	chr5:30346809-30346859	AG04449	skin:	fetal
39	chr5:30346020-30346070	GM12878	blood:	n/a
40	chr5:30346809-30346859	HepG2	liver:	n/a
41	chr5:30346020-30346070	SK-N-SH	brain:	n/a
42	chr5:30346020-30346070	AG09319	gingival:	n/a
43	chr5:30346164-30346214	Hela-S3	cervix:	n/a
44	chr5:30346020-30346070	GM12892	blood:	n/a
45	chr5:30346020-30346070	MCF-7	breast:	n/a
46	chr5:30346020-30346070	HCPEpiC	choroid plexus:	n/a
47	chr5:30346020-30346070	A549	lung:	n/a
48	chr5:30346809-30346859	NB4	blood:	n/a
49	chr5:30346809-30346859	HCM	heart:	n/a
50	chr5:30346809-30346859	U87	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:30278631..30281098-chr5:30286611..30289310,2	MCF-7	breast:
2	chr5:30304961..30306799-chr5:30312361..30314543,2	K562	blood:
3	chr5:30335608..30338399-chr5:30338549..30341547,3	MCF-7	breast:
4	chr5:30335608..30338399-chr5:30338549..30341547,3	MCF-7	breast:
5	chr5:30306752..30308851-chr5:30323163..30325456,2	MCF-7	breast:
6	chr5:30329682..30331741-chr5:30336346..30338195,2	MCF-7	breast:
7	chr5:30329682..30331741-chr5:30336346..30338195,2	MCF-7	breast:
8	chr5:30304961..30306799-chr5:30312361..30314543,2	K562	blood:
9	chr5:30306752..30308851-chr5:30323163..30325456,2	MCF-7	breast:
10	chr5:30222192..30224045-chr5:30226621..30229213,2	MCF-7	breast:
11	chr15:65211077..65211949-chr5:30263002..30263927,2	MCF-7	breast:
12	chr5:30348749..30351521-chr5:30376148..30377890,2	K562	blood:
13	chr5:30352726..30354416-chr5:30354463..30356083,2	MCF-7	breast:
14	chr5:30352726..30354416-chr5:30354463..30356083,2	MCF-7	breast:
15	chr5:30278631..30281098-chr5:30286611..30289310,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-4	chr5:30248457-30249000	NONHSAT100874

No data

Variant related genes	Relation type
ENSG00000250587	TF binding region
ENSG00000250118	TF binding region
ENSG00000250587	CpG island
ENSG00000250118	CpG island

Extended variants
information (count: 1091 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4446473	chr5:30226419-30226420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533635582	chr5:30226456-30226457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191798021	chr5:30226463-30226464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373525387	chr5:30226484-30226485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs16900007	chr5:30226496-30226497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553435122	chr5:30226533-30226534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144481036	chr5:30226539-30226540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534632687	chr5:30226583-30226584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554626666	chr5:30226587-30226588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369749541	chr5:30226603-30226604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574550627	chr5:30226629-30226630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543165628	chr5:30226654-30226655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559670849	chr5:30226679-30226680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577012183	chr5:30226699-30226700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13184068	chr5:30226708-30226709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs559421153	chr5:30226750-30226751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528443824	chr5:30226770-30226771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548148454	chr5:30226878-30226879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545656134	chr5:30226895-30226896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561761710	chr5:30226935-30226936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543257845	chr5:30226954-30226955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530873538	chr5:30226986-30226987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184068985	chr5:30227012-30227013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557182454	chr5:30227022-30227023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550797756	chr5:30227024-30227025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577084316	chr5:30227025-30227026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151121802	chr5:30227043-30227044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547251799	chr5:30227074-30227075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567141968	chr5:30227111-30227112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140916117	chr5:30227113-30227114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149409508	chr5:30236626-30236627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190243513	chr5:30236651-30236652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530385239	chr5:30236704-30236705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550176226	chr5:30236720-30236721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182466406	chr5:30236800-30236801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563809260	chr5:30236811-30236812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561326868	chr5:30236813-30236814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530073655	chr5:30236854-30236855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532840616	chr5:30236918-30236919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144605074	chr5:30236968-30236969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186742542	chr5:30236972-30236973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76561592	chr5:30237010-30237011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74706938	chr5:30237015-30237016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549820174	chr5:30237103-30237104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565977553	chr5:30237124-30237125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs60373268	chr5:30237154-30237155	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs74901492	chr5:30237230-30237231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573557466	chr5:30237248-30237249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10059447	chr5:30237256-30237257	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs556142793	chr5:30237282-30237283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:30226400-30227000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:30227000-30227200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:30236600-30239400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr5:30236800-30237200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:30237200-30237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:30239200-30239400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:30239200-30239600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:30239200-30239800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:30239200-30240000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:30239200-30240000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr5:30239200-30240200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:30239400-30239800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr5:30239400-30240200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr5:30239400-30240200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:30239600-30240200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:30242200-30242400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:30242400-30242800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:30242800-30245400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:30245400-30245800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:30249800-30250200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:30266400-30266600	Enhancers	Fetal Brain Male	brain
22	chr5:30271400-30274400	Enhancers	Hela-S3	cervix
23	chr5:30276200-30276600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:30276400-30277000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:30299000-30299200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:30301800-30310200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:30310400-30310800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:30314600-30315600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:30315400-30315600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:30337400-30337600	Enhancers	Pancreas	Pancrea
31	chr5:30345600-30345800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:30346000-30346400	Active TSS	H1 Cell Line	embryonic stem cell
33	chr5:30346000-30346400	Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr5:30346000-30346400	Active TSS	HSMM	muscle
35	chr5:30346000-30346400	Active TSS	NHEK	skin
36	chr5:30366400-30378800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links