Variant report

Variant	nsv983808
Chromosome Location	chr14:24503854-24523979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:1037)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24505981-24506248	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24505949-24506263	GM12878	blood:	n/a	n/a
3	BACH1	chr14:24520657-24521296	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:24520989-24520990	K562	blood:	n/a	n/a
5	BACH1	chr14:24521710-24521907	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:24506427-24506735	GM12878	blood:	n/a	n/a
7	BATF	chr14:24506432-24506750	GM12878	blood:	n/a	n/a
8	BCL3	chr14:24505902-24506304	A549	lung:	n/a	n/a
9	BHLHE40	chr14:24521140-24521338	K562	blood:	n/a	chr14:24521244-24521260 chr14:24521234-24521250
10	BHLHE40	chr14:24505965-24506313	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:24505981-24506214	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr14:24520957-24521157	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr14:24520977-24521403	K562	blood:	n/a	n/a
14	CEBPB	chr14:24505923-24506358	A549	lung:	n/a	chr14:24506174-24506185
15	CEBPB	chr14:24505949-24506410	HepG2	liver:	n/a	chr14:24506174-24506185
16	CEBPB	chr14:24505919-24506258	H1-hESC	embryonic stem cell:	n/a	chr14:24506174-24506185
17	CEBPB	chr14:24504202-24504207	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr14:24505928-24506341	A549	lung:	n/a	chr14:24506174-24506185
19	CEBPB	chr14:24505955-24506340	MCF-7	breast:	n/a	chr14:24506174-24506185
20	CEBPB	chr14:24505832-24506370	GM12878	blood:	n/a	chr14:24506174-24506185
21	CEBPB	chr14:24505953-24506379	MCF-7	breast:	n/a	chr14:24506174-24506185
22	CEBPB	chr14:24503873-24504233	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:24505530-24505585	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:24505883-24506354	Hela-S3	cervix:	n/a	chr14:24506174-24506185
25	CEBPB	chr14:24503786-24503943	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:24506005-24506241	ECC-1	luminal epithelium:	n/a	chr14:24506174-24506185
27	CEBPB	chr14:24503705-24503975	MCF-7	breast:	n/a	n/a
28	CEBPB	chr14:24505959-24506192	HepG2	liver:	n/a	chr14:24506174-24506185
29	CEBPB	chr14:24504095-24504242	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:24503875-24503956	A549	lung:	n/a	n/a
31	CEBPB	chr14:24506005-24506217	HepG2	liver:	n/a	chr14:24506174-24506185
32	CEBPD	chr14:24520827-24521325	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:24521654-24521938	HepG2	liver:	n/a	n/a
34	CEBPD	chr14:24505867-24506262	HepG2	liver:	n/a	n/a
35	CEBPD	chr14:24520928-24521299	HepG2	liver:	n/a	n/a
36	CEBPD	chr14:24505874-24506366	HepG2	liver:	n/a	n/a
37	CEBPD	chr14:24505308-24505800	HepG2	liver:	n/a	n/a
38	CHD1	chr14:24505868-24506176	GM12878	blood:	n/a	n/a
39	CHD1	chr14:24521650-24521678	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr14:24505969-24506247	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr14:24505991-24506252	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr14:24521055-24521206	H1-hESC	embryonic stem cell:	n/a	chr14:24521179-24521189
43	CHD2	chr14:24520864-24521346	GM12878	blood:	n/a	chr14:24521202-24521212 chr14:24521179-24521189
44	CHD2	chr14:24521059-24521110	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr14:24521645-24521646	HepG2	liver:	n/a	n/a
46	CHD2	chr14:24520888-24521272	K562	blood:	n/a	chr14:24521202-24521212 chr14:24521179-24521189
47	CHD2	chr14:24505468-24505622	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr14:24521565-24521828	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr14:24520889-24521274	HepG2	liver:	n/a	chr14:24521202-24521212 chr14:24521179-24521189
50	CHD2	chr14:24506007-24506172	HepG2	liver:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24520922-24520972	HMEC	breast:	n/a
2	chr14:24520788-24520838	AG10803	skin:	n/a
3	chr14:24505743-24505793	PFSK-1	brain:	n/a
4	chr14:24505671-24505721	H1-hESC	embryonic stem cell:	embryo
5	chr14:24505743-24505793	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:24521434-24521484	MCF-7	breast:	n/a
7	chr14:24505671-24505721	A549	lung:	n/a
8	chr14:24517260-24517310	HCF	heart:	n/a
9	chr14:24520788-24520838	T-47D	breast:	n/a
10	chr14:24505554-24505604	SK-N-SH_RA	brain:	n/a
11	chr14:24517260-24517310	HEEpiC	esophagus:	n/a
12	chr14:24521434-24521484	MCF10A-Er-Src	breast:	n/a
13	chr14:24505547-24505597	GM12878	blood:	n/a
14	chr14:24520922-24520972	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:24506241-24506291	GM12878	blood:	n/a
16	chr14:24506241-24506291	HMEC	breast:	n/a
17	chr14:24520922-24520972	ProgFib	skin:	n/a
18	chr14:24505554-24505604	HL-60	blood:	n/a
19	chr14:24521326-24521376	SKMC	muscle:	n/a
20	chr14:24520788-24520838	RPTEC	kidney:	n/a
21	chr14:24505743-24505793	NB4	blood:	n/a
22	chr14:24505554-24505604	HCPEpiC	choroid plexus:	n/a
23	chr14:24505653-24505703	HIPEpiC	eye:	n/a
24	chr14:24505537-24505587	SKMC	muscle:	n/a
25	chr14:24520922-24520972	Caco-2	colon:	n/a
26	chr14:24520922-24520972	BJ	skin:	n/a
27	chr14:24505547-24505597	HIPEpiC	eye:	n/a
28	chr14:24521326-24521376	AG09309	skin:	n/a
29	chr14:24505554-24505604	BJ	skin:	n/a
30	chr14:24521326-24521376	T-47D	breast:	n/a
31	chr14:24520922-24520972	AG09319	gingival:	n/a
32	chr14:24517260-24517310	GM12891	blood:	n/a
33	chr14:24505537-24505587	BE2_C	brain:	n/a
34	chr14:24505653-24505703	HRE	kidney:	n/a
35	chr14:24521326-24521376	HEK293	kidney:	embryo
36	chr14:24521326-24521376	BJ	skin:	n/a
37	chr14:24505554-24505604	NT2-D1	testis:	n/a
38	chr14:24520788-24520838	Hela-S3	cervix:	n/a
39	chr14:24520922-24520972	NT2-D1	testis:	n/a
40	chr14:24520788-24520838	GM12892	blood:	n/a
41	chr14:24517260-24517310	H1-hESC	embryonic stem cell:	embryo
42	chr14:24517260-24517310	HEK293	kidney:	embryo
43	chr14:24520922-24520972	HAEpiC	amniotic membrane:	n/a
44	chr14:24520788-24520838	HIPEpiC	eye:	n/a
45	chr14:24520788-24520838	GM12891	blood:	n/a
46	chr14:24505537-24505587	HCPEpiC	choroid plexus:	n/a
47	chr14:24521843-24521893	IMR90	lung:	fetal
48	chr14:24505671-24505721	GM12892	blood:	n/a
49	chr14:24505537-24505587	HRPEpiC	eye:	n/a
50	chr14:24509703-24509753	NH-A	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
2	chr14:24519146..24523502-chr14:24549476..24554002,6	MCF-7	breast:
3	chr14:24519494..24523801-chr14:24562244..24565641,8	MCF-7	breast:
4	chr14:24505359..24507247-chr14:24702110..24704400,2	MCF-7	breast:
5	chr14:24511940..24516638-chr14:24519281..24522769,4	MCF-7	breast:
6	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
7	chr14:24519595..24523490-chr14:24615649..24620329,4	MCF-7	breast:
8	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
9	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
10	chr14:24521386..24523883-chr14:24578349..24580057,2	MCF-7	breast:
11	chr14:24523011..24525249-chr14:24526454..24529124,3	K562	blood:
12	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
13	chr14:24523871..24526246-chr14:24529120..24532101,3	MCF-7	breast:
14	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
15	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
16	chr14:24523828..24526460-chr14:24582327..24585206,3	MCF-7	breast:
17	chr14:24519507..24523114-chr14:24581353..24584961,4	MCF-7	breast:
18	chr14:24519379..24521106-chr14:24565277..24567591,2	MCF-7	breast:
19	chr14:24509893..24511543-chr14:24520701..24522909,2	MCF-7	breast:
20	chr14:24519207..24521902-chr14:24608488..24612189,3	MCF-7	breast:
21	chr14:24509752..24511803-chr14:24562900..24565443,2	MCF-7	breast:
22	chr14:24523943..24525993-chr14:24563412..24565144,2	K562	blood:
23	chr14:24520169..24522570-chr14:24571507..24573400,2	MCF-7	breast:
24	chr14:24523943..24525572-chr14:24562582..24565144,2	K562	blood:
25	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
26	chr14:24522487..24524225-chr14:24539392..24540998,2	K562	blood:
27	chr14:24519308..24521603-chr14:24550146..24552325,2	K562	blood:
28	chr14:24521298..24523574-chr14:24582110..24584268,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000225766	TF binding region
LRRC16B	TF binding region
ENSG00000225766	CpG island
LRRC16B	CpG island
ENSG00000100884	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000100938	chromatin interactions
ENSG00000092098	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000100911	chromatin interactions
ENSG00000100908	chromatin interactions
ENSG00000186648	chromatin interactions
ENSG00000259321	chromatin interactions
ENSG00000196943	chromatin interactions

Extended variants
information (count: 1018 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555465437	chr14:24503899-24503900	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs533051155	chr14:24503906-24503907	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs35176785	chr14:24503917-24503918	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs76088845	chr14:24503923-24503924	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs186014064	chr14:24503953-24503954	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs190476731	chr14:24503992-24503993	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs557982061	chr14:24504000-24504001	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4608258	chr14:24504014-24504015	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs529530779	chr14:24504017-24504018	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs528978508	chr14:24504031-24504032	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs550290638	chr14:24504032-24504033	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200894165	chr14:24504041-24504042	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs577810268	chr14:24504042-24504043	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs182632029	chr14:24504064-24504065	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs563606162	chr14:24504106-24504107	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs568844991	chr14:24504107-24504108	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs140436982	chr14:24504121-24504122	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs561782171	chr14:24504157-24504158	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs527758860	chr14:24504175-24504176	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs373372746	chr14:24504181-24504182	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs185401950	chr14:24504188-24504189	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs564299113	chr14:24504196-24504197	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs202011228	chr14:24504248-24504249	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs62000814	chr14:24504253-24504254	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs377433787	chr14:24504263-24504264	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs570341441	chr14:24504266-24504267	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs138070532	chr14:24504297-24504298	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs2021101	chr14:24504309-24504310	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs190836249	chr14:24504326-24504327	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs2012344	chr14:24504360-24504361	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs577711025	chr14:24504373-24504374	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs182709303	chr14:24504376-24504377	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs2012343	chr14:24504380-24504381	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs2332117	chr14:24504391-24504392	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs557898004	chr14:24504411-24504412	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs397832855	chr14:24504424-24504425	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs397833206	chr14:24504428-24504429	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs571310385	chr14:24504431-24504432	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs3049655	chr14:24504444-24504445	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs2011915	chr14:24504455-24504456	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs1885812	chr14:24504459-24504460	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs555812090	chr14:24504460-24504461	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs188792026	chr14:24504470-24504471	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs2332121	chr14:24504548-24504549	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs2332122	chr14:24504592-24504593	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs574052960	chr14:24504601-24504602	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs373383984	chr14:24504616-24504617	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs397843107	chr14:24504622-24504623	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs556941515	chr14:24504627-24504628	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs397833207	chr14:24504628-24504629	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD

Chromatin state (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24501800-24505200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:24501800-24505200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr14:24502000-24504000	Enhancers	Liver	Liver
4	chr14:24502000-24504400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr14:24502000-24505200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:24502000-24505200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr14:24502400-24505400	Weak transcription	HMEC	breast
8	chr14:24502600-24504200	Weak transcription	Hela-S3	cervix
9	chr14:24502600-24505000	Weak transcription	Pancreas	Pancrea
10	chr14:24502600-24505200	Weak transcription	Osteobl	bone
11	chr14:24502600-24505400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr14:24503000-24504000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:24503000-24505000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:24503000-24505000	Enhancers	A549	lung
15	chr14:24503000-24505400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:24503400-24504000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr14:24503400-24504000	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr14:24503400-24504200	Flanking Active TSS	HepG2	liver
19	chr14:24503400-24504400	Weak transcription	Dnd41	blood
20	chr14:24503400-24505200	Enhancers	Fetal Thymus	thymus
21	chr14:24503600-24504000	Enhancers	Adipose Nuclei	Adipose
22	chr14:24503600-24505200	Weak transcription	Psoas Muscle	Psoas
23	chr14:24503600-24505400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr14:24503600-24505600	Weak transcription	NHLF	lung
25	chr14:24503800-24504000	Enhancers	Primary B cells from cord blood	blood
26	chr14:24503800-24505000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr14:24503800-24505000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr14:24503800-24505000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr14:24503800-24505000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr14:24503800-24505000	Weak transcription	Fetal Lung	lung
31	chr14:24503800-24505000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr14:24503800-24505200	Enhancers	Fetal Intestine Large	intestine
33	chr14:24503800-24505200	Weak transcription	Placenta	Placenta
34	chr14:24503800-24505400	Weak transcription	Esophagus	oesophagus
35	chr14:24503800-24505600	Weak transcription	NHDF-Ad	bronchial
36	chr14:24504000-24504200	Enhancers	Fetal Muscle Leg	muscle
37	chr14:24504000-24505000	Weak transcription	Adipose Nuclei	Adipose
38	chr14:24504000-24505000	Weak transcription	Liver	Liver
39	chr14:24504000-24505000	Weak transcription	Colonic Mucosa	Colon
40	chr14:24504000-24505000	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr14:24504000-24505200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr14:24504000-24505200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr14:24504000-24505200	Weak transcription	Brain Angular Gyrus	brain
44	chr14:24504000-24505400	Weak transcription	Primary B cells from cord blood	blood
45	chr14:24504200-24504800	Weak transcription	Fetal Muscle Leg	muscle
46	chr14:24504200-24505000	Enhancers	Fetal Intestine Small	intestine
47	chr14:24504200-24505000	Enhancers	Hela-S3	cervix
48	chr14:24504200-24505000	Enhancers	HepG2	liver
49	chr14:24504200-24505200	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr14:24504400-24505000	Enhancers	Dnd41	blood

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