Variant report

Variant	esv1804444
Chromosome Location	chr5:68812530-68838432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:68814341-68814476	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:68813634-68814094	HepG2	liver:	n/a	chr5:68814018-68814034
3	ATF3	chr5:68812272-68812568	K562	blood:	n/a	n/a
4	BHLHE40	chr5:68823022-68823295	K562	blood:	n/a	n/a
5	BRCA1	chr5:68816958-68817475	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:68813507-68814239	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr5:68816862-68817461	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:68818514-68818731	MCF-7	breast:	n/a	chr5:68818610-68818621
9	CEBPB	chr5:68812306-68812552	HepG2	liver:	n/a	chr5:68812426-68812437
10	CEBPB	chr5:68823244-68823535	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:68812219-68812598	Hela-S3	cervix:	n/a	chr5:68812426-68812437
12	CEBPB	chr5:68813412-68814046	A549	lung:	n/a	chr5:68813936-68813947
13	CEBPB	chr5:68812279-68812698	A549	lung:	n/a	chr5:68812426-68812437
14	CEBPB	chr5:68823192-68823535	K562	blood:	n/a	n/a
15	CEBPB	chr5:68812244-68812584	IMR90	lung:	n/a	chr5:68812426-68812437
16	CEBPB	chr5:68818531-68818660	HepG2	liver:	n/a	chr5:68818610-68818621
17	CEBPB	chr5:68812260-68812575	K562	blood:	n/a	chr5:68812426-68812437
18	CEBPB	chr5:68834723-68834923	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:68812278-68812580	K562	blood:	n/a	chr5:68812426-68812437
20	CEBPB	chr5:68823181-68823660	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:68818510-68818663	A549	lung:	n/a	chr5:68818610-68818621
22	CEBPB	chr5:68812305-68812611	MCF-7	breast:	n/a	chr5:68812426-68812437
23	CEBPB	chr5:68823245-68823491	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:68812261-68812710	HCT-116	colon:	n/a	chr5:68812426-68812437
25	CEBPB	chr5:68816622-68817601	HCT-116	colon:	n/a	chr5:68816730-68816741
26	CEBPB	chr5:68821436-68821696	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:68813456-68814507	Hela-S3	cervix:	n/a	chr5:68813936-68813947
28	CEBPB	chr5:68816404-68817622	HCT-116	colon:	n/a	chr5:68816730-68816741
29	CEBPB	chr5:68812266-68812568	A549	lung:	n/a	chr5:68812426-68812437
30	CEBPB	chr5:68817035-68817420	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:68813413-68814061	HCT-116	colon:	n/a	chr5:68813936-68813947
32	CEBPB	chr5:68816973-68817429	A549	lung:	n/a	n/a
33	CEBPB	chr5:68816523-68816910	MCF-7	breast:	n/a	chr5:68816730-68816741
34	CEBPB	chr5:68823188-68823480	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:68818550-68818697	Hela-S3	cervix:	n/a	chr5:68818610-68818621
36	CEBPB	chr5:68816579-68817601	IMR90	lung:	n/a	chr5:68816730-68816741
37	CEBPB	chr5:68816651-68816848	K562	blood:	n/a	chr5:68816730-68816741
38	CEBPB	chr5:68816638-68816772	HepG2	liver:	n/a	chr5:68816730-68816741
39	CEBPB	chr5:68834691-68834785	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:68812296-68812610	A549	lung:	n/a	chr5:68812426-68812437
41	CEBPB	chr5:68816572-68817603	Hela-S3	cervix:	n/a	chr5:68816730-68816741
42	CEBPB	chr5:68823197-68823519	K562	blood:	n/a	n/a
43	CEBPB	chr5:68818525-68818803	IMR90	lung:	n/a	chr5:68818610-68818621
44	CEBPB	chr5:68823171-68823667	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:68816583-68816872	A549	lung:	n/a	chr5:68816730-68816741
46	CEBPB	chr5:68813392-68814004	MCF-7	breast:	n/a	chr5:68813936-68813947
47	CEBPB	chr5:68823233-68823538	IMR90	lung:	n/a	n/a
48	CEBPB	chr5:68812292-68812540	K562	blood:	n/a	chr5:68812426-68812437
49	CEBPB	chr5:68823213-68823538	A549	lung:	n/a	n/a
50	CEBPB	chr5:68814451-68814472	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:68786843..68790127-chr5:68821932..68828319,7	MCF-7	breast:
2	chr5:68813539..68815320-chr5:68820921..68822712,2	MCF-7	breast:
3	chr5:68808067..68811530-chr5:68811540..68813490,3	MCF-7	breast:
4	chr5:68711082..68712894-chr5:68825364..68828331,2	MCF-7	breast:
5	chr5:68820102..68821620-chr5:68821807..68823888,2	MCF-7	breast:
6	chr5:68791729..68794377-chr5:68827769..68829901,2	MCF-7	breast:
7	chr5:68811437..68815245-chr5:68822688..68826346,4	MCF-7	breast:
8	chr5:68813539..68815320-chr5:68820921..68822712,2	MCF-7	breast:
9	chr5:68811437..68815245-chr5:68822688..68826346,4	MCF-7	breast:
10	chr5:68664276..68666679-chr5:68812958..68815555,2	MCF-7	breast:
11	chr5:68820102..68821620-chr5:68821807..68823888,2	MCF-7	breast:
12	chr5:68787211..68792044-chr5:68819088..68825852,9	MCF-7	breast:

Variant related genes	Relation type
RNU6-724P	TF binding region
ENSG00000238740	TF binding region
OCLN	TF binding region
ENSG00000085231	chromatin interactions
ENSG00000152939	chromatin interactions
ENSG00000197822	chromatin interactions
ENSG00000152942	chromatin interactions

Extended variants
information (count: 604 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34447380	chr5:68812656-68812657	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542401398	chr5:68812703-68812704	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187655449	chr5:68812712-68812713	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35428705	chr5:68812716-68812717	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560569642	chr5:68812728-68812729	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190489064	chr5:68812811-68812812	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552324565	chr5:68812835-68812836	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554289391	chr5:68812888-68812889	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115682688	chr5:68812921-68812922	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551990723	chr5:68812960-68812961	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs114078380	chr5:68812965-68812966	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550452137	chr5:68812966-68812967	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs182985062	chr5:68812992-68812993	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs116323913	chr5:68813022-68813023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs572597043	chr5:68813058-68813059	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547955573	chr5:68813072-68813073	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566458187	chr5:68813086-68813087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs202209882	chr5:68813123-68813124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375545684	chr5:68813135-68813136	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs553810558	chr5:68813141-68813142	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs58026583	chr5:68813142-68813143	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs59867135	chr5:68813143-68813144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs76790823	chr5:68813145-68813146	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559403169	chr5:68813154-68813155	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533868162	chr5:68813177-68813178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28647373	chr5:68813212-68813213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186954169	chr5:68813224-68813225	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555736962	chr5:68813230-68813231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558293940	chr5:68813231-68813232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369129477	chr5:68813269-68813270	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs576766843	chr5:68813303-68813304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189977420	chr5:68813324-68813325	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141232920	chr5:68813373-68813374	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375549312	chr5:68813483-68813484	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548887902	chr5:68813536-68813537	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575137678	chr5:68813538-68813539	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs183351407	chr5:68813560-68813561	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs534619532	chr5:68813562-68813563	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575272945	chr5:68813625-68813626	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs372106558	chr5:68813626-68813627	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114940596	chr5:68813661-68813662	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs150770997	chr5:68813666-68813667	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564363915	chr5:68813693-68813694	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs77453316	chr5:68813698-68813699	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs73772568	chr5:68813732-68813733	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs376114197	chr5:68813747-68813748	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543368614	chr5:68813776-68813777	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562466272	chr5:68813832-68813833	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529905584	chr5:68813838-68813839	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544843332	chr5:68813852-68813853	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	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
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
Acute myeloid leukemia	21251322	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	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68790200-68824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:68793200-68813600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:68799000-68823200	Weak transcription	Placenta	Placenta
4	chr5:68799400-68814200	Weak transcription	Colonic Mucosa	Colon
5	chr5:68799400-68821800	Weak transcription	Fetal Stomach	stomach
6	chr5:68805400-68813000	Weak transcription	Esophagus	oesophagus
7	chr5:68805600-68816400	Weak transcription	GM12878-XiMat	blood
8	chr5:68805600-68821600	Weak transcription	Lung	lung
9	chr5:68805600-68823400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:68805600-68826200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:68805600-68826600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:68806000-68824200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr5:68806400-68826400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:68806800-68816800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:68806800-68821400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr5:68807000-68821400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:68807000-68821600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:68809000-68814200	Weak transcription	Small Intestine	intestine
19	chr5:68809200-68816400	Weak transcription	NHEK	skin
20	chr5:68809200-68817000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr5:68809600-68813400	Weak transcription	NH-A	brain
22	chr5:68809600-68813600	Weak transcription	NHDF-Ad	bronchial
23	chr5:68809600-68814200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr5:68809600-68814600	Weak transcription	Pancreas	Pancrea
25	chr5:68809600-68817200	Weak transcription	NHLF	lung
26	chr5:68809800-68812600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr5:68809800-68816600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr5:68810000-68812800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr5:68810000-68813400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr5:68810400-68812600	Weak transcription	HepG2	liver
31	chr5:68810400-68815200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr5:68810400-68815600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:68810400-68815600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr5:68810400-68821600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr5:68810400-68821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:68810400-68823600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr5:68812000-68812600	Strong transcription	Fetal Intestine Small	intestine
38	chr5:68812000-68813000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:68812000-68813400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:68812200-68812800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:68812200-68815200	Enhancers	Hela-S3	cervix
42	chr5:68812200-68818000	Enhancers	Stomach Mucosa	stomach
43	chr5:68812400-68812800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:68812400-68813000	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr5:68812400-68813400	Enhancers	A549	lung
46	chr5:68812400-68813800	Enhancers	HMEC	breast
47	chr5:68812400-68814400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr5:68812400-68814400	Enhancers	HUVEC	blood vessel
49	chr5:68812400-68814600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:68812400-68814600	Enhancers	Muscle Satellite Cultured Cells	--

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