Variant report

Variant	nsv1019763
Chromosome Location	chr5:120284495-120544707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:123)
Chromatin interactive
region (count:26)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	ARID3A	chr5:120480659-120480718	K562	blood:	n/a	n/a
3	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
4	CBX3	chr5:120289176-120289482	K562	blood:	n/a	n/a
5	CEBPB	chr5:120497807-120498101	IMR90	lung:	n/a	chr5:120497966-120497977
6	CEBPB	chr5:120489382-120489687	HepG2	liver:	n/a	chr5:120489508-120489519
7	CEBPB	chr5:120344890-120345090	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:120313457-120313761	A549	lung:	n/a	chr5:120313575-120313586
9	CEBPB	chr5:120321723-120321990	HepG2	liver:	n/a	chr5:120321831-120321842
10	CEBPB	chr5:120489328-120489659	H1-hESC	embryonic stem cell:	n/a	chr5:120489508-120489519
11	CEBPB	chr5:120497839-120498066	HepG2	liver:	n/a	chr5:120497966-120497977
12	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
14	CEBPB	chr5:120518774-120519213	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:120511816-120512016	HepG2	liver:	n/a	chr5:120511903-120511914
16	CEBPB	chr5:120518614-120519156	HepG2	liver:	n/a	chr5:120518723-120518734
17	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
18	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
19	CEBPB	chr5:120362842-120363162	H1-hESC	embryonic stem cell:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
20	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
21	CEBPB	chr5:120324365-120324487	K562	blood:	n/a	n/a
22	CEBPB	chr5:120500288-120500607	K562	blood:	n/a	n/a
23	CEBPB	chr5:120534992-120535592	Hela-S3	cervix:	n/a	chr5:120534993-120535006
24	CEBPB	chr5:120497904-120498020	A549	lung:	n/a	chr5:120497966-120497977
25	CEBPB	chr5:120510128-120510341	K562	blood:	n/a	n/a
26	CEBPB	chr5:120518649-120519214	A549	lung:	n/a	chr5:120518723-120518734
27	CEBPB	chr5:120497794-120498111	K562	blood:	n/a	chr5:120497966-120497977
28	CEBPB	chr5:120315991-120316249	HepG2	liver:	n/a	chr5:120316125-120316136
29	CEBPB	chr5:120518577-120518857	K562	blood:	n/a	chr5:120518723-120518734
30	CEBPB	chr5:120489377-120489704	K562	blood:	n/a	chr5:120489508-120489519
31	CEBPB	chr5:120489367-120489679	A549	lung:	n/a	chr5:120489508-120489519
32	CEBPB	chr5:120362833-120363079	IMR90	lung:	n/a	chr5:120362980-120362991
33	CEBPB	chr5:120465336-120465526	K562	blood:	n/a	chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447 chr5:120465434-120465445 chr5:120465434-120465447 chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447
34	CEBPB	chr5:120386141-120386392	A549	lung:	n/a	chr5:120386256-120386267
35	CEBPB	chr5:120509430-120509502	K562	blood:	n/a	chr5:120509449-120509462 chr5:120509449-120509460
36	CEBPB	chr5:120313451-120313786	HepG2	liver:	n/a	chr5:120313575-120313586
37	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
39	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
40	CEBPB	chr5:120321709-120321907	HepG2	liver:	n/a	chr5:120321831-120321842
41	CEBPB	chr5:120313455-120313746	K562	blood:	n/a	chr5:120313575-120313586
42	CEBPB	chr5:120362854-120363100	A549	lung:	n/a	chr5:120362980-120362991
43	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
44	CEBPB	chr5:120344818-120345134	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:120535010-120535378	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
47	CEBPB	chr5:120325504-120325793	A549	lung:	n/a	chr5:120325601-120325614
48	CEBPB	chr5:120344767-120345102	A549	lung:	n/a	n/a
49	CEBPD	chr5:120480469-120480757	K562	blood:	n/a	n/a
50	CEBPD	chr5:120480488-120480808	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120444080-120444130	HAEpiC	amniotic membrane:	n/a
2	chr5:120444080-120444130	HAEpiC	amniotic membrane:	n/a
3	chr5:120444080-120444130	HepG2	liver:	n/a
4	chr5:120400115-120400165	HIPEpiC	eye:	n/a
5	chr5:120400115-120400165	CMK	blood:	n/a
6	chr5:120444080-120444130	AoSMC	blood vessel:	n/a
7	chr5:120400115-120400165	U87	brain:	n/a
8	chr5:120400115-120400165	Caco-2	colon:	n/a
9	chr5:120400115-120400165	SK-N-MC	brain:	n/a
10	chr5:120444080-120444130	AG04449	skin:	fetal
11	chr5:120400115-120400165	GM12891	blood:	n/a
12	chr5:120444080-120444130	GM19239	blood:	n/a
13	chr5:120400115-120400165	GM06990	blood:	n/a
14	chr5:120400115-120400165	Hepatocyte	liver:	n/a
15	chr5:120400115-120400165	AG09319	gingival:	n/a
16	chr5:120444080-120444130	BJ	skin:	n/a
17	chr5:120444080-120444130	HCF	heart:	n/a
18	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
19	chr5:120444080-120444130	SAEC	small airway:	n/a
20	chr5:120400115-120400165	AG04449	skin:	fetal
21	chr5:120444080-120444130	AG09309	skin:	n/a
22	chr5:120400115-120400165	AG09309	skin:	n/a
23	chr5:120444080-120444130	HEEpiC	esophagus:	n/a
24	chr5:120444080-120444130	PANC-1	pancreas:	n/a
25	chr5:120444080-120444130	SK-N-SH_RA	brain:	n/a
26	chr5:120444080-120444130	HL-60	blood:	n/a
27	chr5:120400115-120400165	HCT-116	colon:	n/a
28	chr5:120400115-120400165	PrEC	prostate:	n/a
29	chr5:120444080-120444130	HMEC	breast:	n/a
30	chr5:120400115-120400165	NH-A	brain:	n/a
31	chr5:120400115-120400165	Hela-S3	cervix:	n/a
32	chr5:120444080-120444130	U87	brain:	n/a
33	chr5:120444080-120444130	Jurkat	blood:	n/a
34	chr5:120400115-120400165	ProgFib	skin:	n/a
35	chr5:120400115-120400165	PFSK-1	brain:	n/a
36	chr5:120444080-120444130	Hepatocyte	liver:	n/a
37	chr5:120444080-120444130	HIPEpiC	eye:	n/a
38	chr5:120400115-120400165	BJ	skin:	n/a
39	chr5:120400115-120400165	BE2_C	brain:	n/a
40	chr5:120400115-120400165	T-47D	breast:	n/a
41	chr5:120444080-120444130	MCF10A-Er-Src	breast:	n/a
42	chr5:120400115-120400165	ECC-1	luminal epithelium:	n/a
43	chr5:120400115-120400165	K562	blood:	n/a
44	chr5:120444080-120444130	NT2-D1	testis:	n/a
45	chr5:120444080-120444130	PFSK-1	brain:	n/a
46	chr5:120444080-120444130	NB4	blood:	n/a
47	chr5:120400115-120400165	A549	lung:	n/a
48	chr5:120400115-120400165	PANC-1	pancreas:	n/a
49	chr5:120400115-120400165	NT2-D1	testis:	n/a
50	chr5:120400115-120400165	HPAEpiC	pulmonary alveolar:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
2	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
3	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
4	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
5	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
6	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
7	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
8	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
9	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
10	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
11	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
12	chr5:120300949..120302956-chr5:121296548..121298304,2	K562	blood:
13	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
14	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
15	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
16	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
17	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
18	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
19	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
20	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
21	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
22	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
23	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
24	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
25	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
26	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
2	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
3	lnc-FTMT-2	chr5:120535399-120535503	ENSG00000229855.4
4	lnc-FTMT-2	chr5:120540703-120540825	ENSG00000229855.4
5	lnc-LOX-8	chr5:120531675-120531905	NONHSAT103452
6	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
7	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
8	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450

No data

Variant related genes	Relation type
ENSG00000229855	TF binding region
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000250847	TF binding region
ENSG00000229855	CpG island
ENSG00000251135	CpG island
ENSG00000248853	CpG island
ENSG00000250847	CpG island
ENSG00000151304	chromatin interactions

Extended variants
information (count: 6017 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6017 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374276346	chr5:120284526-120284527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182464688	chr5:120284574-120284575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78800192	chr5:120284583-120284584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542073082	chr5:120284607-120284608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13436660	chr5:120284609-120284610	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs79200928	chr5:120284652-120284653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530197024	chr5:120284695-120284696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549483615	chr5:120284727-120284728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564460538	chr5:120284785-120284786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185370835	chr5:120284786-120284787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549831246	chr5:120284787-120284788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561883197	chr5:120284817-120284818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190266245	chr5:120284937-120284938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181553058	chr5:120284942-120284943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566149387	chr5:120284971-120284972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540076468	chr5:120284986-120284987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371285676	chr5:120285031-120285032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551807697	chr5:120285064-120285065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570391697	chr5:120285065-120285066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185896160	chr5:120285084-120285085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556271618	chr5:120285146-120285147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75600767	chr5:120285157-120285158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs137907363	chr5:120285168-120285169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535635960	chr5:120285194-120285195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190168436	chr5:120285195-120285196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572152127	chr5:120285219-120285220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79210658	chr5:120285270-120285271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564241029	chr5:120285319-120285320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373499782	chr5:120285326-120285327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576371576	chr5:120285328-120285329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181000403	chr5:120285330-120285331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561846013	chr5:120285339-120285340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529305445	chr5:120285367-120285368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547486754	chr5:120285380-120285381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559867517	chr5:120285400-120285401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533375924	chr5:120285444-120285445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569907315	chr5:120285482-120285483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1833645	chr5:120285489-120285490	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186153903	chr5:120285528-120285529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368211536	chr5:120285565-120285566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190675493	chr5:120285575-120285576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568072605	chr5:120285577-120285578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535497105	chr5:120285584-120285585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553608704	chr5:120285643-120285644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140160738	chr5:120285651-120285652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539291573	chr5:120285656-120285657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184064640	chr5:120285710-120285711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2909937	chr5:120285718-120285719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114819052	chr5:120285776-120285777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561698106	chr5:120285794-120285795	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:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120273400-120289200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:120279000-120286600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:120279400-120284600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:120284600-120284800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr5:120284600-120285000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr5:120284600-120285600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:120284600-120285600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr5:120285000-120285200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:120285200-120285600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:120289200-120289800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:120289200-120290000	ZNF genes & repeats	Dnd41	blood
12	chr5:120289600-120290000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:120293400-120293600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:120293600-120294400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:120294400-120296200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:120302000-120302800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:120302600-120302800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:120302800-120312200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:120316200-120316600	Enhancers	Fetal Brain Male	brain
20	chr5:120321000-120324600	Bivalent Enhancer	Fetal Lung	lung
21	chr5:120324000-120324200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:120324200-120324800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:120324200-120325400	Enhancers	Dnd41	blood
24	chr5:120324600-120326200	Enhancers	Fetal Lung	lung
25	chr5:120324800-120325000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:120324800-120326600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:120325400-120327400	Weak transcription	Dnd41	blood
28	chr5:120326400-120326800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:120326600-120327200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:120327000-120327400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:120327200-120327400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:120327400-120328200	Enhancers	Dnd41	blood
33	chr5:120328200-120334000	Weak transcription	Dnd41	blood
34	chr5:120334000-120334200	Enhancers	Dnd41	blood
35	chr5:120334200-120337600	Weak transcription	Dnd41	blood
36	chr5:120338600-120340600	Enhancers	Dnd41	blood
37	chr5:120340200-120341000	Enhancers	HUVEC	blood vessel
38	chr5:120340600-120343600	Weak transcription	Dnd41	blood
39	chr5:120343600-120345600	Strong transcription	Dnd41	blood
40	chr5:120343800-120345800	Bivalent Enhancer	Fetal Heart	heart
41	chr5:120344400-120344800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr5:120345600-120347000	Weak transcription	Dnd41	blood
43	chr5:120347000-120347400	Enhancers	Dnd41	blood
44	chr5:120347400-120348600	Weak transcription	Dnd41	blood
45	chr5:120348600-120348800	Enhancers	Dnd41	blood
46	chr5:120348800-120349000	Genic enhancers	Dnd41	blood
47	chr5:120349000-120350200	Weak transcription	Dnd41	blood
48	chr5:120350200-120351800	Enhancers	Dnd41	blood
49	chr5:120351800-120352200	Active TSS	Dnd41	blood
50	chr5:120352200-120352600	Flanking Active TSS	Dnd41	blood

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