Variant report

Variant	nsv1032799
Chromosome Location	chr5:115533065-115609552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
2	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
4	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
5	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
6	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
8	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
9	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
10	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
11	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
12	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
13	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
15	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
16	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
17	CTCF	chr5:115573680-115573830	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr5:115608400-115608550	GM12868	blood:	n/a	n/a
19	CTCF	chr5:115608000-115608150	GM12872	blood:	n/a	n/a
20	CTCF	chr5:115608320-115608470	Caco-2	colon:	n/a	n/a
21	CTCF	chr5:115573740-115573890	BJ	skin:	n/a	n/a
22	CTCF	chr5:115608420-115608570	HPF	lung:	n/a	n/a
23	CTCF	chr5:115608420-115608570	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr5:115608400-115608550	GM06990	blood:	n/a	n/a
25	CTCF	chr5:115608320-115608470	RPTEC	kidney:	n/a	n/a
26	CTCF	chr5:115608320-115608470	HCM	heart:	n/a	n/a
27	CTCF	chr5:115608440-115608590	AG04450	lung:	n/a	n/a
28	CTCF	chr5:115573695-115573940	IMR90	lung:	n/a	n/a
29	CTCF	chr5:115573720-115573870	GM06990	blood:	n/a	n/a
30	CTCF	chr5:115573660-115573970	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:115573640-115573790	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr5:115608380-115608530	GM12866	blood:	n/a	n/a
33	CTCF	chr5:115608440-115608590	GM12869	blood:	n/a	n/a
34	CTCF	chr5:115608380-115608530	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr5:115608400-115608550	AG04450	lung:	n/a	n/a
36	CTCF	chr5:115608400-115608550	HPF	lung:	n/a	n/a
37	CTCF	chr5:115608372-115608591	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:115608380-115608530	AG09309	skin:	n/a	n/a
39	CTCF	chr5:115608400-115608550	GM12878	blood:	n/a	n/a
40	CTCF	chr5:115608400-115608550	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr5:115608300-115608450	GM12874	blood:	n/a	n/a
42	CTCF	chr5:115608380-115608530	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr5:115573740-115573890	SAEC	small airway:	n/a	n/a
44	CTCF	chr5:115608380-115608530	BE2_C	brain:	n/a	n/a
45	CTCF	chr5:115573660-115573810	AG04450	lung:	n/a	n/a
46	CTCF	chr5:115573739-115573920	GM12878	blood:	n/a	n/a
47	CTCF	chr5:115573700-115573850	GM12872	blood:	n/a	n/a
48	CTCF	chr5:115608340-115608490	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr5:115608380-115608530	GM12868	blood:	n/a	n/a
50	CTCF	chr5:115573740-115573890	GM12864	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	HIPEpiC	eye:	n/a
2	chr5:115599680-115599730	HIPEpiC	eye:	n/a
3	chr5:115599680-115599730	HCT-116	colon:	n/a
4	chr5:115599680-115599730	Jurkat	blood:	n/a
5	chr5:115599680-115599730	PANC-1	pancreas:	n/a
6	chr5:115599680-115599730	HRPEpiC	eye:	n/a
7	chr5:115599680-115599730	GM06990	blood:	n/a
8	chr5:115599680-115599730	SAEC	small airway:	n/a
9	chr5:115599680-115599730	Hela-S3	cervix:	n/a
10	chr5:115599680-115599730	LNCaP	prostate:	n/a
11	chr5:115599680-115599730	GM12891	blood:	n/a
12	chr5:115599680-115599730	SK-N-SH	brain:	n/a
13	chr5:115599680-115599730	T-47D	breast:	n/a
14	chr5:115599680-115599730	GM19239	blood:	n/a
15	chr5:115599680-115599730	SK-N-MC	brain:	n/a
16	chr5:115599680-115599730	HCM	heart:	n/a
17	chr5:115599680-115599730	AG04450	lung:	fetal
18	chr5:115599680-115599730	IMR90	lung:	fetal
19	chr5:115599680-115599730	CMK	blood:	n/a
20	chr5:115599680-115599730	AG10803	skin:	n/a
21	chr5:115599680-115599730	HL-60	blood:	n/a
22	chr5:115599680-115599730	U87	brain:	n/a
23	chr5:115599680-115599730	HUVEC	blood vessel:	n/a
24	chr5:115599680-115599730	Caco-2	colon:	n/a
25	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
26	chr5:115599680-115599730	K562	blood:	n/a
27	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
28	chr5:115599680-115599730	PrEC	prostate:	n/a
29	chr5:115599680-115599730	AG09309	skin:	n/a
30	chr5:115599680-115599730	A549	lung:	n/a
31	chr5:115599680-115599730	NB4	blood:	n/a
32	chr5:115599680-115599730	HRE	kidney:	n/a
33	chr5:115599680-115599730	HCF	heart:	n/a
34	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
35	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
36	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
37	chr5:115599680-115599730	HEK293	kidney:	embryo
38	chr5:115599680-115599730	GM12892	blood:	n/a
39	chr5:115599680-115599730	RPTEC	kidney:	n/a
40	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
41	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
42	chr5:115599680-115599730	NT2-D1	testis:	n/a
43	chr5:115599680-115599730	HepG2	liver:	n/a
44	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
46	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
47	chr5:115599680-115599730	Hepatocyte	liver:	n/a
48	chr5:115599680-115599730	MCF-7	breast:	n/a
49	chr5:115599680-115599730	HMEC	breast:	n/a
50	chr5:115599680-115599730	PFSK-1	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
2	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
3	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
4	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
5	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LVRN.1-3	chr5:115549572-115550152	NONHSAT103355
2	lnc-SEMA6A-7	chr5:115553723-115553992	NONHSAT103356

No data

Variant related genes	Relation type
HMGN2P27	TF binding region
HMGN2P27	CpG island
ENSG00000212457	chromatin interactions

Extended variants
information (count: 3964 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3964 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4921078	chr5:115533065-115533066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149484481	chr5:115533147-115533148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375039413	chr5:115533159-115533160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10037305	chr5:115533165-115533166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs557163454	chr5:115533172-115533173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576870092	chr5:115533173-115533174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541553339	chr5:115533186-115533187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183626378	chr5:115533216-115533217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559628068	chr5:115533239-115533240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573165497	chr5:115533265-115533266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145926008	chr5:115533270-115533271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562334130	chr5:115533289-115533290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530995960	chr5:115533290-115533291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56252845	chr5:115533312-115533313	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563190409	chr5:115533322-115533323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188619177	chr5:115533324-115533325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73257267	chr5:115533331-115533332	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566004309	chr5:115533332-115533333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534946680	chr5:115533334-115533335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139820333	chr5:115533337-115533338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563866805	chr5:115533340-115533341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73257269	chr5:115533341-115533342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs111316336	chr5:115533357-115533358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143451459	chr5:115533403-115533404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10037375	chr5:115533407-115533408	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs146280646	chr5:115533428-115533429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371734290	chr5:115533451-115533452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73257272	chr5:115533456-115533457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs148453635	chr5:115533495-115533496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73257274	chr5:115533523-115533524	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7449449	chr5:115533546-115533547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs113377919	chr5:115533554-115533555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535148330	chr5:115533577-115533578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575798401	chr5:115533581-115533582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62384233	chr5:115533597-115533598	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs116710890	chr5:115533602-115533603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532219688	chr5:115533618-115533619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539743292	chr5:115533628-115533629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6859442	chr5:115533633-115533634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192530797	chr5:115533634-115533635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62384234	chr5:115533645-115533646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548507535	chr5:115533656-115533657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568213795	chr5:115533659-115533660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530739992	chr5:115533669-115533670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373771392	chr5:115533671-115533672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556893910	chr5:115533683-115533684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150985115	chr5:115533704-115533705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376756662	chr5:115533728-115533729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140478506	chr5:115533737-115533738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371326943	chr5:115533763-115533764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115481400-115536000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr5:115509600-115533400	Weak transcription	HSMM	muscle
3	chr5:115511800-115533200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:115518800-115548000	Weak transcription	Psoas Muscle	Psoas
5	chr5:115522200-115536000	Weak transcription	Primary B cells from cord blood	blood
6	chr5:115522400-115538000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr5:115522600-115536800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:115522600-115540200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr5:115524400-115536800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:115525800-115560000	Weak transcription	Left Ventricle	heart
11	chr5:115527800-115539000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr5:115527800-115543800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:115528600-115536800	Weak transcription	Primary T cells from cord blood	blood
14	chr5:115529000-115539200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:115533200-115533600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:115533600-115538400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:115535400-115537000	Weak transcription	Fetal Intestine Large	intestine
18	chr5:115535400-115537600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr5:115536000-115537200	Strong transcription	Primary B cells from cord blood	blood
20	chr5:115536000-115537400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr5:115536600-115537000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr5:115536800-115537000	Enhancers	Pancreas	Pancrea
23	chr5:115536800-115537200	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr5:115536800-115537400	Strong transcription	Primary T cells from cord blood	blood
25	chr5:115536800-115537600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
26	chr5:115537000-115537200	ZNF genes & repeats	Fetal Intestine Large	intestine
27	chr5:115537000-115538200	Weak transcription	Pancreas	Pancrea
28	chr5:115537200-115537400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
29	chr5:115537200-115537600	Strong transcription	Fetal Intestine Large	intestine
30	chr5:115537200-115559400	Weak transcription	Primary B cells from cord blood	blood
31	chr5:115537400-115539600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr5:115537400-115545000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr5:115537400-115560000	Weak transcription	Primary T cells from cord blood	blood
34	chr5:115537600-115542400	Weak transcription	Fetal Intestine Large	intestine
35	chr5:115537600-115560200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr5:115542600-115562800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:115543200-115543800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr5:115543800-115545800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:115544000-115544400	Enhancers	Ovary	ovary
40	chr5:115545800-115549600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:115547400-115548000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:115547400-115548200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:115548000-115548200	Enhancers	Psoas Muscle	Psoas
44	chr5:115549600-115550400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:115549800-115560000	Weak transcription	Fetal Intestine Small	intestine
46	chr5:115550400-115556400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:115551800-115576400	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr5:115553400-115560200	Weak transcription	Fetal Stomach	stomach
49	chr5:115555000-115555800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:115555000-115557200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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