Variant report

Variant	nsv428125
Chromosome Location	chr5:120194868-120458466
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:427)
Chromatin interactive
region (count:19)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120321426-120321583	HepG2	liver:	n/a	n/a
2	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
3	CBX3	chr5:120289176-120289482	K562	blood:	n/a	n/a
4	CEBPB	chr5:120254653-120255046	HCT-116	colon:	n/a	n/a
5	CEBPB	chr5:120208128-120208204	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
7	CEBPB	chr5:120344767-120345102	A549	lung:	n/a	n/a
8	CEBPB	chr5:120254719-120255091	A549	lung:	n/a	n/a
9	CEBPB	chr5:120260572-120260815	K562	blood:	n/a	chr5:120260680-120260691
10	CEBPB	chr5:120243945-120244154	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:120362854-120363100	A549	lung:	n/a	chr5:120362980-120362991
12	CEBPB	chr5:120254751-120255081	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:120206319-120206613	HepG2	liver:	n/a	chr5:120206461-120206472
14	CEBPB	chr5:120203027-120203285	HepG2	liver:	n/a	chr5:120203173-120203184
15	CEBPB	chr5:120236959-120237290	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:120254721-120255092	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:120321709-120321907	HepG2	liver:	n/a	chr5:120321831-120321842
18	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
19	CEBPB	chr5:120344890-120345090	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:120254817-120255040	K562	blood:	n/a	n/a
21	CEBPB	chr5:120203111-120203312	H1-hESC	embryonic stem cell:	n/a	chr5:120203173-120203184
22	CEBPB	chr5:120321723-120321990	HepG2	liver:	n/a	chr5:120321831-120321842
23	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:120254734-120255092	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:120386141-120386392	A549	lung:	n/a	chr5:120386256-120386267
26	CEBPB	chr5:120362833-120363079	IMR90	lung:	n/a	chr5:120362980-120362991
27	CEBPB	chr5:120254745-120255040	K562	blood:	n/a	n/a
28	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
29	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:120208105-120208305	HepG2	liver:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245
31	CEBPB	chr5:120313451-120313786	HepG2	liver:	n/a	chr5:120313575-120313586
32	CEBPB	chr5:120260548-120260826	HepG2	liver:	n/a	chr5:120260680-120260691
33	CEBPB	chr5:120254718-120255097	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
35	CEBPB	chr5:120209949-120209981	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:120254753-120255060	MCF-7	breast:	n/a	n/a
37	CEBPB	chr5:120254722-120255094	K562	blood:	n/a	n/a
38	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
39	CEBPB	chr5:120362842-120363162	H1-hESC	embryonic stem cell:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
40	CEBPB	chr5:120313455-120313746	K562	blood:	n/a	chr5:120313575-120313586
41	CEBPB	chr5:120313457-120313761	A549	lung:	n/a	chr5:120313575-120313586
42	CEBPB	chr5:120344818-120345134	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:120254788-120255079	A549	lung:	n/a	n/a
44	CEBPB	chr5:120203065-120203348	K562	blood:	n/a	chr5:120203173-120203184
45	CEBPB	chr5:120324365-120324487	K562	blood:	n/a	n/a
46	CEBPB	chr5:120315991-120316249	HepG2	liver:	n/a	chr5:120316125-120316136
47	CEBPB	chr5:120254692-120255072	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr5:120218188-120218329	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:120208117-120208321	A549	lung:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245
50	CEBPB	chr5:120325504-120325793	A549	lung:	n/a	chr5:120325601-120325614

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120278165-120278215	Hepatocyte	liver:	n/a
2	chr5:120272625-120272675	GM19239	blood:	n/a
3	chr5:120278165-120278215	HRCEpiC	kidney:	n/a
4	chr5:120400115-120400165	BJ	skin:	n/a
5	chr5:120272574-120272624	IMR90	lung:	fetal
6	chr5:120272574-120272624	BJ	skin:	n/a
7	chr5:120254714-120254764	HRPEpiC	eye:	n/a
8	chr5:120444080-120444130	NHDF-neo	bronchial:	n/a
9	chr5:120444080-120444130	HCM	heart:	n/a
10	chr5:120272574-120272624	T-47D	breast:	n/a
11	chr5:120444080-120444130	AG04449	skin:	fetal
12	chr5:120248381-120248431	HNPCEpiC	eye:	n/a
13	chr5:120248381-120248431	NHDF-neo	bronchial:	n/a
14	chr5:120278165-120278215	BE2_C	brain:	n/a
15	chr5:120278165-120278215	NT2-D1	testis:	n/a
16	chr5:120278165-120278215	GM12891	blood:	n/a
17	chr5:120248381-120248431	HRE	kidney:	n/a
18	chr5:120272625-120272675	A549	lung:	n/a
19	chr5:120272574-120272624	GM12878	blood:	n/a
20	chr5:120254714-120254764	ECC-1	luminal epithelium:	n/a
21	chr5:120254714-120254764	HRCEpiC	kidney:	n/a
22	chr5:120444080-120444130	HAEpiC	amniotic membrane:	n/a
23	chr5:120272574-120272624	AoSMC	blood vessel:	n/a
24	chr5:120272574-120272624	SK-N-SH	brain:	n/a
25	chr5:120272574-120272624	HCM	heart:	n/a
26	chr5:120254714-120254764	NHBE	bronchial:	n/a
27	chr5:120248381-120248431	BJ	skin:	n/a
28	chr5:120400115-120400165	PFSK-1	brain:	n/a
29	chr5:120248381-120248431	Hepatocyte	liver:	n/a
30	chr5:120278165-120278215	SK-N-SH_RA	brain:	n/a
31	chr5:120248381-120248431	NT2-D1	testis:	n/a
32	chr5:120444080-120444130	PANC-1	pancreas:	n/a
33	chr5:120278165-120278215	HL-60	blood:	n/a
34	chr5:120272574-120272624	ECC-1	luminal epithelium:	n/a
35	chr5:120272625-120272675	PrEC	prostate:	n/a
36	chr5:120272625-120272675	PANC-1	pancreas:	n/a
37	chr5:120272625-120272675	K562	blood:	n/a
38	chr5:120278165-120278215	GM19239	blood:	n/a
39	chr5:120272574-120272624	NH-A	brain:	n/a
40	chr5:120444080-120444130	SK-N-SH_RA	brain:	n/a
41	chr5:120272574-120272624	MCF10A-Er-Src	breast:	n/a
42	chr5:120248381-120248431	NB4	blood:	n/a
43	chr5:120400115-120400165	PANC-1	pancreas:	n/a
44	chr5:120444080-120444130	AG09309	skin:	n/a
45	chr5:120272574-120272624	CMK	blood:	n/a
46	chr5:120272625-120272675	Hela-S3	cervix:	n/a
47	chr5:120254714-120254764	CMK	blood:	n/a
48	chr5:120278165-120278215	K562	blood:	n/a
49	chr5:120254714-120254764	HMEC	breast:	n/a
50	chr5:120444080-120444130	SK-N-MC	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
2	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
3	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
4	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
5	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:
6	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
7	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
8	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
9	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
10	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
11	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
12	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
13	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
14	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
15	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
16	chr5:120300949..120302956-chr5:121296548..121298304,2	K562	blood:
17	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:
18	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
19	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
2	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
3	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
4	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450
5	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450

No data

Variant related genes	Relation type
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000251135	CpG island
ENSG00000248853	CpG island
ENSG00000151304	chromatin interactions

Extended variants
information (count: 6131 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6131 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370861995	chr5:120194892-120194893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13189918	chr5:120194939-120194940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs182649593	chr5:120194980-120194981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201251369	chr5:120195012-120195013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529853548	chr5:120195034-120195035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548389083	chr5:120195042-120195043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560417154	chr5:120195098-120195099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541285150	chr5:120195101-120195102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188934430	chr5:120195108-120195109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552413987	chr5:120195157-120195158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376195215	chr5:120195217-120195218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192477412	chr5:120195258-120195259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10077418	chr5:120195380-120195381	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184433967	chr5:120195384-120195385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187311985	chr5:120195390-120195391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549916330	chr5:120195469-120195470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146369367	chr5:120195476-120195477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553927957	chr5:120195511-120195512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572280205	chr5:120195553-120195554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372468232	chr5:120195583-120195584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539650951	chr5:120195588-120195589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138311709	chr5:120195622-120195623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576708572	chr5:120195633-120195634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544185115	chr5:120195786-120195787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149647558	chr5:120195799-120195800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144226141	chr5:120195804-120195805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111279247	chr5:120195826-120195827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191930955	chr5:120195841-120195842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184858105	chr5:120195864-120195865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375103868	chr5:120195885-120195886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12522824	chr5:120195916-120195917	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs189659644	chr5:120195963-120195964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530577097	chr5:120195983-120195984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148728414	chr5:120195991-120195992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144718011	chr5:120196007-120196008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374881271	chr5:120196022-120196023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570397671	chr5:120196110-120196111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147471753	chr5:120196154-120196155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568146566	chr5:120196175-120196176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538981624	chr5:120196191-120196192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529273889	chr5:120196193-120196194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547442608	chr5:120196200-120196201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192496164	chr5:120196203-120196204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540017805	chr5:120196210-120196211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566014581	chr5:120196222-120196223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536498319	chr5:120196250-120196251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139991633	chr5:120196256-120196257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116315302	chr5:120196284-120196285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28729806	chr5:120196292-120196293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs184471458	chr5:120196350-120196351	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
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120193000-120199800	Weak transcription	Fetal Lung	lung
2	chr5:120194000-120196000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:120199800-120200200	Enhancers	Fetal Lung	lung
4	chr5:120200000-120203000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr5:120202800-120203000	Enhancers	Dnd41	blood
6	chr5:120203000-120203200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:120203000-120203200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr5:120203000-120203400	Flanking Active TSS	Dnd41	blood
9	chr5:120203000-120204600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:120203000-120204600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:120203000-120204600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:120203000-120204800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:120203200-120203400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr5:120203200-120203400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr5:120203200-120203400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:120203200-120204200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr5:120203200-120204200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr5:120203400-120204000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr5:120203400-120204000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:120203400-120206000	Enhancers	Dnd41	blood
21	chr5:120203600-120204200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr5:120204000-120204400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr5:120204000-120204600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:120204200-120204400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:120204200-120204600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:120204200-120204600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr5:120205600-120205800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:120207600-120207800	Enhancers	Fetal Brain Male	brain
29	chr5:120207600-120210000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:120207600-120210400	Enhancers	Fetal Lung	lung
31	chr5:120208000-120210200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:120208600-120209800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:120208800-120209200	Enhancers	HUVEC	blood vessel
34	chr5:120222200-120222400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:120222200-120222600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:120222400-120227400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:120227400-120227800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:120228000-120228200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:120236800-120237600	Enhancers	Dnd41	blood
40	chr5:120246200-120246800	Enhancers	Fetal Lung	lung
41	chr5:120246600-120247000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:120247000-120249000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:120248400-120248800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:120248800-120254200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr5:120249000-120249400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:120249000-120249400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:120249000-120249400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:120249400-120253000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:120249400-120253000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:120253000-120253400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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