Variant report

Variant	nsv598325
Chromosome Location	chr5:61436505-61468051
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	CEBPB	chr5:61466469-61466739	IMR90	lung:	n/a	n/a
2	CEBPB	chr5:61459905-61460138	K562	blood:	n/a	n/a
3	CEBPB	chr5:61466571-61466632	K562	blood:	n/a	n/a
4	CEBPB	chr5:61465307-61465380	HepG2	liver:	n/a	chr5:61465317-61465328
5	CTCF	chr5:61442440-61442590	GM12865	blood:	n/a	n/a
6	CTCF	chr5:61439592-61439754	MCF-7	breast:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
7	CTCF	chr5:61439573-61439821	Gliobla	brain:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
8	CTCF	chr5:61439840-61439990	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr5:61439640-61439790	K562	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661
10	CTCF	chr5:61439580-61439730	GM12864	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
11	CTCF	chr5:61439620-61439770	HFF-Myc	foreskin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
12	CTCF	chr5:61439560-61439710	AG04449	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
13	CTCF	chr5:61439620-61439770	GM12864	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
14	CTCF	chr5:61439620-61439770	NHEK	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
15	CTCF	chr5:61439600-61439750	GM06990	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
16	CTCF	chr5:61440220-61440370	AG09309	skin:	n/a	n/a
17	CTCF	chr5:61465042-61465132	A549	lung:	n/a	chr5:61465055-61465063
18	CTCF	chr5:61439800-61439950	GM12866	blood:	n/a	n/a
19	CTCF	chr5:61439820-61439970	GM12872	blood:	n/a	n/a
20	CTCF	chr5:61439580-61439730	AG09319	gingival:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
21	CTCF	chr5:61439458-61439853	GM12878	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
22	CTCF	chr5:61439100-61439250	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr5:61439571-61439758	Lung_OC	lung:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
24	CTCF	chr5:61439900-61440050	AG04450	lung:	n/a	n/a
25	CTCF	chr5:61439640-61439790	GM12873	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661
26	CTCF	chr5:61439620-61439770	AoAF	blood vessel:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
27	CTCF	chr5:61439543-61439778	GM12878	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
28	CTCF	chr5:61439560-61439777	GM13977	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
29	CTCF	chr5:61440400-61440550	HCFaa	heart:	n/a	n/a
30	CTCF	chr5:61439520-61439670	GM12870	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
31	CTCF	chr5:61439614-61439745	GM20000	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
32	CTCF	chr5:61439500-61439650	HepG2	liver:	n/a	n/a
33	CTCF	chr5:61439540-61439690	NHEK	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
34	CTCF	chr5:61439600-61439750	GM12878	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
35	CTCF	chr5:61439460-61439610	HAc	cerebellar:	n/a	n/a
36	CTCF	chr5:61439560-61439710	HEK293	kidney:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
37	CTCF	chr5:61439560-61439710	GM12871	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
38	CTCF	chr5:61439560-61439710	SAEC	small airway:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
39	CTCF	chr5:61439552-61439772	LNCaP	prostate:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
40	CTCF	chr5:61439560-61439710	HPAF	blood vessel:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
41	CTCF	chr5:61439580-61439730	HPAF	blood vessel:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
42	CTCF	chr5:61439600-61439750	HRE	kidney:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
43	CTCF	chr5:61439540-61439690	GM12875	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
44	CTCF	chr5:61439462-61439809	A549	lung:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
45	CTCF	chr5:61439549-61439762	Pancreas_OC	pancreas:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
46	CTCF	chr5:61439510-61439734	SK-N-SH_RA	brain:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
47	CTCF	chr5:61439575-61439762	Kidney_OC	kidney:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
48	CTCF	chr5:61464963-61465169	K562	blood:	n/a	chr5:61465055-61465063
49	CTCF	chr5:61439540-61439690	BJ	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
50	CTCF	chr5:61439560-61439710	GM12865	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61439790-61439840	K562	blood:	n/a
2	chr5:61439790-61439840	HCT-116	colon:	n/a
3	chr5:61439790-61439840	BJ	skin:	n/a
4	chr5:61439790-61439840	AG09309	skin:	n/a
5	chr5:61439790-61439840	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:61439790-61439840	GM06990	blood:	n/a
7	chr5:61439790-61439840	T-47D	breast:	n/a
8	chr5:61439790-61439840	SK-N-SH_RA	brain:	n/a
9	chr5:61439790-61439840	HRCEpiC	kidney:	n/a
10	chr5:61439790-61439840	HIPEpiC	eye:	n/a
11	chr5:61439790-61439840	HEEpiC	esophagus:	n/a
12	chr5:61439790-61439840	HCPEpiC	choroid plexus:	n/a
13	chr5:61439790-61439840	HRE	kidney:	n/a
14	chr5:61439790-61439840	HEK293	kidney:	embryo
15	chr5:61439790-61439840	HepG2	liver:	n/a
16	chr5:61439790-61439840	AG04450	lung:	fetal
17	chr5:61439790-61439840	ProgFib	skin:	n/a
18	chr5:61439790-61439840	LNCaP	prostate:	n/a
19	chr5:61439790-61439840	HUVEC	blood vessel:	n/a
20	chr5:61439790-61439840	GM12891	blood:	n/a
21	chr5:61439790-61439840	NHDF-neo	bronchial:	n/a
22	chr5:61439790-61439840	A549	lung:	n/a
23	chr5:61439790-61439840	AG10803	skin:	n/a
24	chr5:61439790-61439840	Jurkat	blood:	n/a
25	chr5:61439790-61439840	GM19239	blood:	n/a
26	chr5:61439790-61439840	HMEC	breast:	n/a
27	chr5:61439790-61439840	NH-A	brain:	n/a
28	chr5:61439790-61439840	ECC-1	luminal epithelium:	n/a
29	chr5:61439790-61439840	U87	brain:	n/a
30	chr5:61439790-61439840	HAEpiC	amniotic membrane:	n/a
31	chr5:61439790-61439840	Caco-2	colon:	n/a
32	chr5:61439790-61439840	RPTEC	kidney:	n/a
33	chr5:61439790-61439840	MCF10A-Er-Src	breast:	n/a
34	chr5:61439790-61439840	PFSK-1	brain:	n/a
35	chr5:61439790-61439840	NT2-D1	testis:	n/a
36	chr5:61439790-61439840	ovcar-3	ovarian:	n/a
37	chr5:61439790-61439840	HCF	heart:	n/a
38	chr5:61439790-61439840	Hepatocyte	liver:	n/a
39	chr5:61439790-61439840	NB4	blood:	n/a
40	chr5:61439790-61439840	SKMC	muscle:	n/a
41	chr5:61439790-61439840	GM12878	blood:	n/a
42	chr5:61439790-61439840	BE2_C	brain:	n/a
43	chr5:61439790-61439840	GM12892	blood:	n/a
44	chr5:61439790-61439840	MCF-7	breast:	n/a
45	chr5:61439790-61439840	Hela-S3	cervix:	n/a
46	chr5:61439790-61439840	NHBE	bronchial:	n/a
47	chr5:61439790-61439840	AG04449	skin:	fetal
48	chr5:61439790-61439840	SAEC	small airway:	n/a
49	chr5:61439790-61439840	AG09319	gingival:	n/a
50	chr5:61439790-61439840	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:61422681..61424219-chr5:61436524..61438145,2	MCF-7	breast:
2	chr5:61442438..61445370-chr5:61445571..61447544,2	MCF-7	breast:
3	chr12:125398291..125400539-chr5:61461576..61463918,2	MCF-7	breast:
4	chr5:61229619..61230608-chr5:61439489..61440182,2	MCF-7	breast:
5	chr5:61439485..61439993-chr5:61501806..61502567,2	MCF-7	breast:
6	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:
7	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF2A-2	chr5:61442492-61442773	NONHSAT101705

Variant related genes	Relation type
RN7SKP157	TF binding region
RN7SKP157	CpG island
ENSG00000265345	chromatin interactions
ENSG00000251983	chromatin interactions
ENSG00000150991	chromatin interactions

Extended variants
information (count: 601 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:601 , 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	rs2962027	chr5:61436505-61436506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183995411	chr5:61436509-61436510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534812711	chr5:61436524-61436525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554661880	chr5:61436525-61436526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568198952	chr5:61436526-61436527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368721993	chr5:61436535-61436536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537040915	chr5:61436584-61436585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564512172	chr5:61436623-61436624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115565958	chr5:61436633-61436634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577450922	chr5:61436665-61436666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs67090804	chr5:61436670-61436671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs398093429	chr5:61436671-61436672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546441034	chr5:61436686-61436687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568193011	chr5:61436758-61436759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554422182	chr5:61436859-61436860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187622627	chr5:61436885-61436886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192196977	chr5:61436909-61436910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542059500	chr5:61436967-61436968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561843983	chr5:61436995-61436996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79247432	chr5:61437030-61437031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544186782	chr5:61437038-61437039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564473518	chr5:61437085-61437086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535599395	chr5:61437105-61437106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184185886	chr5:61437135-61437136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552399645	chr5:61437165-61437166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565842950	chr5:61437185-61437186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188589209	chr5:61437216-61437217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371154825	chr5:61437223-61437224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142176325	chr5:61437231-61437232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191634492	chr5:61437236-61437237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537175607	chr5:61437277-61437278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs397883446	chr5:61437286-61437287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547465814	chr5:61437335-61437336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556794291	chr5:61437354-61437355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184529128	chr5:61437384-61437385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12657078	chr5:61437433-61437434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558403208	chr5:61437452-61437453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189356936	chr5:61437472-61437473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144360635	chr5:61437509-61437510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115003829	chr5:61437538-61437539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147804011	chr5:61437569-61437570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs148841674	chr5:61437596-61437597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576372560	chr5:61437640-61437641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11746415	chr5:61437645-61437646	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs573779649	chr5:61437687-61437688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372948323	chr5:61437709-61437710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182244290	chr5:61437822-61437823	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs374396670	chr5:61437843-61437844	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs565235178	chr5:61437847-61437848	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs73114102	chr5:61437852-61437853	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Non-small cell lung cancer	21829676	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
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	20729466	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
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61434600-61437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:61434600-61439200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:61435000-61441600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:61435200-61437800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr5:61435200-61438000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:61435200-61438000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:61435200-61438200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:61435400-61438200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr5:61435800-61437800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:61435800-61438200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr5:61435800-61438400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr5:61436000-61436800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:61436000-61437200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:61436800-61437200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:61437200-61438000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:61437200-61439600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:61437600-61438400	Enhancers	Fetal Kidney	kidney
18	chr5:61437800-61438000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:61437800-61438000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:61437800-61438600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:61437800-61439800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:61437800-61440600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr5:61438000-61438200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:61438000-61438400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:61438000-61438600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:61438000-61438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:61438000-61439400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr5:61438000-61440400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr5:61438000-61440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:61438200-61438600	Enhancers	Aorta	Aorta
31	chr5:61438200-61440000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr5:61438200-61440400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:61438200-61440800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:61438400-61439400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:61438400-61439400	Enhancers	Brain Cingulate Gyrus	brain
36	chr5:61438400-61439400	Enhancers	Brain Hippocampus Middle	brain
37	chr5:61438400-61439400	Weak transcription	Fetal Kidney	kidney
38	chr5:61438400-61440400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr5:61438600-61439000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:61438600-61439000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:61438600-61439200	Weak transcription	Aorta	Aorta
42	chr5:61438600-61440800	Enhancers	Brain Substantia Nigra	brain
43	chr5:61438800-61439200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:61438800-61439800	Enhancers	Brain Angular Gyrus	brain
45	chr5:61438800-61440800	Enhancers	Brain Anterior Caudate	brain
46	chr5:61439000-61439400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:61439000-61439400	Enhancers	Stomach Smooth Muscle	stomach
48	chr5:61439000-61440200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:61439000-61440800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:61439200-61439400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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