Variant report

Variant	nsv969994
Chromosome Location	chr5:74314591-74330479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:72)
CpG islands
(count:305)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:72 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:74317260-74317368	K562	blood:	n/a	n/a
2	CEBPB	chr5:74330447-74330568	HepG2	liver:	n/a	n/a
3	CEBPB	chr5:74330260-74330713	MCF-7	breast:	n/a	n/a
4	CTCF	chr5:74326991-74327057	GM13976	blood:	n/a	n/a
5	CTCF	chr5:74321880-74322030	HMF	breast:	n/a	n/a
6	CTCF	chr5:74323672-74323744	GM13976	blood:	n/a	n/a
7	CTCF	chr5:74316060-74316210	GM12866	blood:	n/a	n/a
8	CTCF	chr5:74317543-74317547	GM13976	blood:	n/a	n/a
9	CTCF	chr5:74317469-74317539	GM13976	blood:	n/a	n/a
10	CTCF	chr5:74315900-74316050	HepG2	liver:	n/a	n/a
11	EP300	chr5:74315728-74316198	HepG2	liver:	n/a	n/a
12	FOSL2	chr5:74315737-74316190	HepG2	liver:	n/a	chr5:74315949-74315960
13	FOSL2	chr5:74315792-74316121	HepG2	liver:	n/a	chr5:74315949-74315960
14	FOXA1	chr5:74317580-74317941	HepG2	liver:	n/a	n/a
15	FOXA1	chr5:74315783-74316223	HepG2	liver:	n/a	n/a
16	FOXA1	chr5:74317603-74318028	HepG2	liver:	n/a	n/a
17	HNF4A	chr5:74315810-74316137	HepG2	liver:	n/a	n/a
18	JUND	chr5:74315833-74316039	HepG2	liver:	n/a	n/a
19	JUND	chr5:74315812-74316046	HepG2	liver:	n/a	n/a
20	MAFF	chr5:74317216-74317509	HepG2	liver:	n/a	n/a
21	MAFF	chr5:74315791-74316120	HepG2	liver:	n/a	n/a
22	MAFK	chr5:74328363-74328491	HepG2	liver:	n/a	chr5:74328418-74328434 chr5:74328419-74328433 chr5:74328416-74328436
23	MAFK	chr5:74317222-74317475	HepG2	liver:	n/a	n/a
24	MAFK	chr5:74315847-74316094	HepG2	liver:	n/a	n/a
25	MAFK	chr5:74317197-74317486	HepG2	liver:	n/a	n/a
26	MAFK	chr5:74315785-74316169	HepG2	liver:	n/a	n/a
27	MAFK	chr5:74323511-74323688	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAX	chr5:74319790-74319864	NB4	blood:	n/a	chr5:74319811-74319821
29	MAX	chr5:74316152-74316293	HepG2	liver:	n/a	n/a
30	MAZ	chr5:74325309-74325474	HepG2	liver:	n/a	n/a
31	MXI1	chr5:74319786-74319867	H1-hESC	embryonic stem cell:	n/a	chr5:74319812-74319821
32	MYBL2	chr5:74315710-74316179	HepG2	liver:	n/a	n/a
33	MYC	chr5:74315945-74316162	MCF-7	breast:	n/a	n/a
34	MYC	chr5:74319716-74319740	MCF10A-Er-Src	breast:	n/a	n/a
35	MYC	chr5:74316056-74316155	MCF-7	breast:	n/a	n/a
36	NFIC	chr5:74315753-74316236	HepG2	liver:	n/a	n/a
37	NFIC	chr5:74315858-74316142	HepG2	liver:	n/a	n/a
38	POLR2A	chr5:74328145-74328548	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr5:74322457-74322461	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr5:74316056-74316338	MCF-7	breast:	n/a	n/a
41	POLR2A	chr5:74326918-74326985	MCF-7	breast:	n/a	n/a
42	POLR2A	chr5:74323607-74323807	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr5:74316354-74316363	MCF-7	breast:	n/a	n/a
44	POLR2A	chr5:74316115-74316286	HepG2	liver:	n/a	n/a
45	POLR2A	chr5:74327282-74327410	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr5:74316234-74316347	MCF-7	breast:	n/a	n/a
47	POLR2A	chr5:74315105-74315166	ProgFib	skin:	n/a	n/a
48	POLR2A	chr5:74316072-74316334	A549	lung:	n/a	n/a
49	POLR2A	chr5:74314769-74314793	Gliobla	brain:	n/a	n/a
50	STAT3	chr5:74330468-74330543	MCF10A-Er-Src	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74326281-74326331	HRE	kidney:	n/a
2	chr5:74327277-74327327	GM12892	blood:	n/a
3	chr5:74327281-74327331	CMK	blood:	n/a
4	chr5:74330425-74330475	H1-hESC	embryonic stem cell:	embryo
5	chr5:74327277-74327327	AG09309	skin:	n/a
6	chr5:74327281-74327331	SKMC	muscle:	n/a
7	chr5:74327281-74327331	HUVEC	blood vessel:	n/a
8	chr5:74327277-74327327	NB4	blood:	n/a
9	chr5:74326281-74326331	MCF10A-Er-Src	breast:	n/a
10	chr5:74328211-74328261	SK-N-MC	brain:	n/a
11	chr5:74327281-74327331	SK-N-SH_RA	brain:	n/a
12	chr5:74330425-74330475	BE2_C	brain:	n/a
13	chr5:74326281-74326331	SKMC	muscle:	n/a
14	chr5:74326281-74326331	HEEpiC	esophagus:	n/a
15	chr5:74327281-74327331	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:74330425-74330475	RPTEC	kidney:	n/a
17	chr5:74326281-74326331	SK-N-SH	brain:	n/a
18	chr5:74328211-74328261	HNPCEpiC	eye:	n/a
19	chr5:74327277-74327327	HCM	heart:	n/a
20	chr5:74326281-74326331	RPTEC	kidney:	n/a
21	chr5:74327281-74327331	AG04449	skin:	fetal
22	chr5:74327281-74327331	T-47D	breast:	n/a
23	chr5:74326281-74326331	Caco-2	colon:	n/a
24	chr5:74330425-74330475	SKMC	muscle:	n/a
25	chr5:74327277-74327327	RPTEC	kidney:	n/a
26	chr5:74326281-74326331	PrEC	prostate:	n/a
27	chr5:74326281-74326331	PANC-1	pancreas:	n/a
28	chr5:74327277-74327327	HRPEpiC	eye:	n/a
29	chr5:74328211-74328261	HUVEC	blood vessel:	n/a
30	chr5:74330425-74330475	LNCaP	prostate:	n/a
31	chr5:74326281-74326331	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:74330425-74330475	SK-N-SH	brain:	n/a
33	chr5:74327281-74327331	AG09309	skin:	n/a
34	chr5:74326281-74326331	K562	blood:	n/a
35	chr5:74330425-74330475	CMK	blood:	n/a
36	chr5:74328211-74328261	MCF10A-Er-Src	breast:	n/a
37	chr5:74327281-74327331	AoSMC	blood vessel:	n/a
38	chr5:74327277-74327327	SAEC	small airway:	n/a
39	chr5:74327277-74327327	NT2-D1	testis:	n/a
40	chr5:74326281-74326331	AG10803	skin:	n/a
41	chr5:74326281-74326331	AG09319	gingival:	n/a
42	chr5:74330425-74330475	HNPCEpiC	eye:	n/a
43	chr5:74328211-74328261	MCF-7	breast:	n/a
44	chr5:74326281-74326331	BE2_C	brain:	n/a
45	chr5:74328211-74328261	GM19239	blood:	n/a
46	chr5:74328211-74328261	GM12878	blood:	n/a
47	chr5:74327281-74327331	HepG2	liver:	n/a
48	chr5:74328211-74328261	K562	blood:	n/a
49	chr5:74327281-74327331	HCT-116	colon:	n/a
50	chr5:74327281-74327331	GM12878	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:57561542..57564393-chr5:74329604..74332106,2	MCF-7	breast:
2	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
3	chr5:74330454..74335475-chr5:74336350..74340630,5	MCF-7	breast:
4	chr5:74315578..74317119-chr5:74341476..74343130,2	MCF-7	breast:
5	chr5:74318809..74320982-chr5:74323765..74325406,2	MCF-7	breast:
6	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
7	chr5:73980015..73981765-chr5:74329525..74332329,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCNT4-1	chr5:74319656-74319753	ENSG00000249856.1

No data

Variant related genes	Relation type
GCNT4	TF binding region
ENSG00000249856	TF binding region
GCNT4	CpG island
ENSG00000249856	CpG island
ENSG00000249856	chromatin interactions
ENSG00000049860	chromatin interactions

Extended variants
information (count: 587 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7736471	chr5:74314658-74314659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568309923	chr5:74314731-74314732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533507544	chr5:74314743-74314744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116152155	chr5:74314744-74314745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544548088	chr5:74314837-74314838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561171526	chr5:74314869-74314870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183838765	chr5:74314878-74314879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7706858	chr5:74314884-74314885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79703518	chr5:74314940-74314941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144703554	chr5:74314947-74314948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374390114	chr5:74314951-74314952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34065076	chr5:74314953-74314954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577003386	chr5:74315015-74315016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370135456	chr5:74315059-74315060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141539628	chr5:74315079-74315080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538163035	chr5:74315088-74315089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140794811	chr5:74315105-74315106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376144575	chr5:74315106-74315107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188565392	chr5:74315164-74315165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181600055	chr5:74315275-74315276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536339801	chr5:74315293-74315294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73112721	chr5:74315338-74315339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs576295475	chr5:74315414-74315415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572996748	chr5:74315418-74315419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114234565	chr5:74315436-74315437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558481778	chr5:74315456-74315457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371704631	chr5:74315540-74315541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575490832	chr5:74315574-74315575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544219733	chr5:74315588-74315589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561318727	chr5:74315600-74315601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574767161	chr5:74315605-74315606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367965967	chr5:74315667-74315668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540252472	chr5:74315704-74315705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145665090	chr5:74315753-74315754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151107235	chr5:74315771-74315772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186727182	chr5:74315809-74315810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367587282	chr5:74315811-74315812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562989184	chr5:74315857-74315858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192033804	chr5:74315930-74315931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548637172	chr5:74315946-74315947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567233351	chr5:74316010-74316011	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs536226230	chr5:74316095-74316096	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546634205	chr5:74316099-74316100	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs181978502	chr5:74316101-74316102	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs141055717	chr5:74316102-74316103	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs35383934	chr5:74316111-74316112	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs538785935	chr5:74316200-74316201	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs558706647	chr5:74316209-74316210	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs575382731	chr5:74316210-74316211	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs114209607	chr5:74316220-74316221	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74303600-74316000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:74313400-74314600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr5:74313600-74318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:74313600-74341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:74314200-74315200	Enhancers	NHDF-Ad	bronchial
6	chr5:74314600-74314800	Enhancers	Pancreas	Pancrea
7	chr5:74314600-74314800	Enhancers	NHLF	lung
8	chr5:74314600-74315200	Enhancers	NH-A	brain
9	chr5:74314600-74324800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:74314800-74315800	Weak transcription	Pancreas	Pancrea
11	chr5:74315000-74315200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:74315200-74315400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:74315200-74315400	Enhancers	Fetal Intestine Large	intestine
14	chr5:74315200-74320400	Enhancers	Stomach Mucosa	stomach
15	chr5:74315200-74332800	Weak transcription	NHDF-Ad	bronchial
16	chr5:74315400-74316200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:74315600-74317000	Weak transcription	Fetal Intestine Large	intestine
18	chr5:74315600-74318000	Enhancers	HepG2	liver
19	chr5:74315800-74316200	Enhancers	Duodenum Mucosa	Duodenum
20	chr5:74315800-74317400	Enhancers	Pancreas	Pancrea
21	chr5:74316000-74316200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:74316000-74316200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr5:74316000-74316400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr5:74316000-74316400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:74316000-74316400	Enhancers	Placenta	Placenta
26	chr5:74316000-74317400	Enhancers	Gastric	stomach
27	chr5:74316000-74317400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr5:74316200-74316400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:74316200-74319400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr5:74316200-74319600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:74316200-74324200	Weak transcription	Duodenum Mucosa	Duodenum
32	chr5:74316400-74317600	Enhancers	Ovary	ovary
33	chr5:74316400-74318800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:74316400-74328000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:74316400-74328200	Weak transcription	Placenta	Placenta
36	chr5:74316400-74330200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:74317000-74317200	Enhancers	Fetal Intestine Large	intestine
38	chr5:74317000-74317400	Enhancers	Fetal Intestine Small	intestine
39	chr5:74317000-74319200	Weak transcription	Primary T cells from cord blood	blood
40	chr5:74317200-74317400	Enhancers	Primary T cells fromperipheralblood	blood
41	chr5:74317200-74317400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr5:74317200-74318000	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr5:74317200-74331400	Weak transcription	Fetal Intestine Large	intestine
44	chr5:74317400-74317600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr5:74317400-74317800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr5:74317400-74319600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr5:74317400-74319600	Weak transcription	Pancreas	Pancrea
48	chr5:74317400-74323800	Weak transcription	Gastric	stomach
49	chr5:74317400-74326800	Weak transcription	Fetal Intestine Small	intestine
50	chr5:74317600-74344200	Weak transcription	Ovary	ovary

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