Variant report

Variant	nsv518286
Chromosome Location	chr5:74169045-74243120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1467)
CpG islands
(count:183)
Chromatin interactive
region (count:23)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74212565-74213265	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74230706-74231126	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:74242220-74242714	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74172145-74172641	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74199250-74199532	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74215365-74215608	K562	blood:	n/a	n/a
7	ARID3A	chr5:74172998-74174476	HepG2	liver:	n/a	chr5:74173359-74173375
8	ARID3A	chr5:74215018-74215648	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:74213940-74214467	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:74221773-74221800	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:74234202-74234415	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:74169725-74170191	HepG2	liver:	n/a	n/a
13	BACH1	chr5:74230915-74231125	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr5:74241372-74241684	GM12878	blood:	n/a	n/a
15	BATF	chr5:74185356-74185778	GM12878	blood:	n/a	n/a
16	BATF	chr5:74185298-74185833	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:74185389-74185810	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:74185499-74185768	GM12878	blood:	n/a	n/a
19	BCLAF1	chr5:74241342-74241682	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:74173641-74174153	HepG2	liver:	n/a	n/a
21	BHLHE40	chr5:74172034-74172630	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:74214018-74214392	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:74212289-74213217	HepG2	liver:	n/a	n/a
24	BHLHE40	chr5:74199321-74199400	GM12878	blood:	n/a	n/a
25	CEBPB	chr5:74230705-74230952	HepG2	liver:	n/a	chr5:74230818-74230831
26	CEBPB	chr5:74212619-74212989	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:74191683-74192219	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr5:74211413-74211593	K562	blood:	n/a	n/a
29	CEBPB	chr5:74213925-74214345	HepG2	liver:	n/a	chr5:74214092-74214105
30	CEBPB	chr5:74170387-74170678	HepG2	liver:	n/a	chr5:74170544-74170555
31	CEBPB	chr5:74211403-74211576	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:74213982-74214247	HepG2	liver:	n/a	chr5:74214092-74214105
33	CEBPB	chr5:74212575-74213077	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:74213867-74214370	HepG2	liver:	n/a	chr5:74214092-74214105
35	CEBPB	chr5:74199116-74199495	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:74212559-74213070	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:74170590-74170591	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:74234222-74234272	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:74219035-74219190	K562	blood:	n/a	n/a
40	CEBPB	chr5:74212478-74213142	MCF-7	breast:	n/a	n/a
41	CEBPB	chr5:74234499-74234641	K562	blood:	n/a	n/a
42	CEBPB	chr5:74212518-74213138	MCF-7	breast:	n/a	n/a
43	CEBPB	chr5:74211479-74211616	A549	lung:	n/a	n/a
44	CEBPB	chr5:74191824-74192241	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr5:74212590-74213020	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:74234101-74234437	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:74213923-74214511	HepG2	liver:	n/a	chr5:74214092-74214105
48	CEBPB	chr5:74230634-74231001	HepG2	liver:	n/a	chr5:74230818-74230831
49	CEBPB	chr5:74173305-74173811	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:74211376-74211658	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74231171-74231221	MCF-7	breast:	n/a
2	chr5:74172353-74172403	GM12891	blood:	n/a
3	chr5:74199422-74199472	CMK	blood:	n/a
4	chr5:74231171-74231221	HRE	kidney:	n/a
5	chr5:74231171-74231221	HCF	heart:	n/a
6	chr5:74231171-74231221	GM12891	blood:	n/a
7	chr5:74199422-74199472	HMEC	breast:	n/a
8	chr5:74172353-74172403	NH-A	brain:	n/a
9	chr5:74231171-74231221	HL-60	blood:	n/a
10	chr5:74172353-74172403	HEK293	kidney:	embryo
11	chr5:74199422-74199472	AG04450	lung:	fetal
12	chr5:74172353-74172403	AoSMC	blood vessel:	n/a
13	chr5:74199422-74199472	Jurkat	blood:	n/a
14	chr5:74199422-74199472	SK-N-SH	brain:	n/a
15	chr5:74172353-74172403	HCPEpiC	choroid plexus:	n/a
16	chr5:74231171-74231221	AG09309	skin:	n/a
17	chr5:74199422-74199472	K562	blood:	n/a
18	chr5:74199422-74199472	ovcar-3	ovarian:	n/a
19	chr5:74199422-74199472	H1-hESC	embryonic stem cell:	embryo
20	chr5:74199422-74199472	GM12891	blood:	n/a
21	chr5:74172353-74172403	SAEC	small airway:	n/a
22	chr5:74199422-74199472	HCT-116	colon:	n/a
23	chr5:74199422-74199472	NHDF-neo	bronchial:	n/a
24	chr5:74199422-74199472	HepG2	liver:	n/a
25	chr5:74231171-74231221	A549	lung:	n/a
26	chr5:74231171-74231221	PANC-1	pancreas:	n/a
27	chr5:74199422-74199472	PFSK-1	brain:	n/a
28	chr5:74199422-74199472	AG09319	gingival:	n/a
29	chr5:74199422-74199472	HEK293	kidney:	embryo
30	chr5:74231171-74231221	CMK	blood:	n/a
31	chr5:74231171-74231221	ProgFib	skin:	n/a
32	chr5:74172353-74172403	Caco-2	colon:	n/a
33	chr5:74231171-74231221	U87	brain:	n/a
34	chr5:74231171-74231221	SAEC	small airway:	n/a
35	chr5:74199422-74199472	GM06990	blood:	n/a
36	chr5:74231171-74231221	SK-N-SH_RA	brain:	n/a
37	chr5:74231171-74231221	RPTEC	kidney:	n/a
38	chr5:74172353-74172403	Hepatocyte	liver:	n/a
39	chr5:74231171-74231221	GM12878	blood:	n/a
40	chr5:74172353-74172403	ECC-1	luminal epithelium:	n/a
41	chr5:74231171-74231221	GM12892	blood:	n/a
42	chr5:74199422-74199472	HAEpiC	amniotic membrane:	n/a
43	chr5:74199422-74199472	GM12892	blood:	n/a
44	chr5:74231171-74231221	NHDF-neo	bronchial:	n/a
45	chr5:74231171-74231221	HRPEpiC	eye:	n/a
46	chr5:74172353-74172403	HUVEC	blood vessel:	n/a
47	chr5:74231171-74231221	IMR90	lung:	fetal
48	chr5:74231171-74231221	HEK293	kidney:	embryo
49	chr5:74199422-74199472	ECC-1	luminal epithelium:	n/a
50	chr5:74172353-74172403	BE2_C	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:73979354..73981671-chr5:74212696..74216316,3	MCF-7	breast:
2	chr5:74221093..74221795-chr5:74230378..74230940,2	MCF-7	breast:
3	chr5:74160756..74162981-chr5:74168227..74170471,2	MCF-7	breast:
4	chr5:74230558..74231547-chr5:74561170..74561749,2	MCF-7	breast:
5	chr5:74161003..74163055-chr5:74170808..74173347,2	MCF-7	breast:
6	chr5:74235381..74238008-chr5:74240552..74242250,2	K562	blood:
7	chr5:74221093..74221795-chr5:74230378..74230940,2	MCF-7	breast:
8	chr5:74185368..74187105-chr5:74187423..74188982,2	MCF-7	breast:
9	chr5:74235381..74238008-chr5:74240552..74242250,2	K562	blood:
10	chr5:73968444..73969362-chr5:74215054..74216242,3	MCF-7	breast:
11	chr5:74230526..74231383-chr5:74345361..74346008,2	MCF-7	breast:
12	chr5:74082489..74083391-chr5:74199247..74199809,4	MCF-7	breast:
13	chr5:73944427..73945323-chr5:74215021..74215775,2	MCF-7	breast:
14	chr5:73980895..73982599-chr5:74214365..74217155,2	MCF-7	breast:
15	chr5:74220860..74221763-chr5:74345733..74346235,2	MCF-7	breast:
16	chr5:74213877..74216591-chr7:112090452..112092226,2	MCF-7	breast:
17	chr5:74185368..74187105-chr5:74187423..74188982,2	MCF-7	breast:
18	chr5:74161211..74163484-chr5:74166665..74169792,3	K562	blood:
19	chr5:74062152..74062829-chr5:74198970..74199641,2	K562	blood:
20	chr5:74239354..74241176-chr5:74242869..74245249,2	MCF-7	breast:
21	chr5:74230538..74231300-chr5:74561168..74561757,3	MCF-7	breast:
22	chr5:74239354..74241176-chr5:74242869..74245249,2	MCF-7	breast:
23	chr5:74220830..74221511-chr5:74561645..74562178,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCNT4-1	chr5:74213551-74213803	ENSG00000249856.1
2	lnc-FAM169A-1	chr5:74199354-74199389	XLOC_004889
3	lnc-NSA2-7	chr5:74225705-74226391	NONHSAT102186
4	lnc-FAM169A-1	chr5:74195136-74195344	XLOC_004889
5	lnc-GCNT4-1	chr5:74214854-74215111	ENSG00000249856.1

No data

Variant related genes	Relation type
ENSG00000239517	TF binding region
ENSG00000212363	TF binding region
ENSG00000196390	TF binding region
ENSG00000239517	CpG island
ENSG00000212363	CpG island
ENSG00000196390	CpG island
ENSG00000198780	chromatin interactions
ENSG00000164346	chromatin interactions
ENSG00000049860	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000271714	chromatin interactions

Extended variants
information (count: 2430 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2430 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10062244	chr5:74169045-74169046	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529758738	chr5:74169078-74169079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540606786	chr5:74169125-74169126	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560544293	chr5:74169153-74169154	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146106357	chr5:74169164-74169165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372501310	chr5:74169215-74169216	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138841241	chr5:74169218-74169219	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs529006304	chr5:74169233-74169234	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531770112	chr5:74169260-74169261	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376366278	chr5:74169277-74169278	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs55886622	chr5:74169327-74169328	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534224822	chr5:74169372-74169373	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546236197	chr5:74169389-74169390	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559629995	chr5:74169427-74169428	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538304483	chr5:74169474-74169475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs550079053	chr5:74169494-74169495	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181468419	chr5:74169495-74169496	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575278305	chr5:74169504-74169505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538004472	chr5:74169508-74169509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554827635	chr5:74169513-74169514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs574741949	chr5:74169524-74169525	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs540544138	chr5:74169530-74169531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560229938	chr5:74169531-74169532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34483827	chr5:74169544-74169545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570199969	chr5:74169567-74169568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186104266	chr5:74169578-74169579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528265771	chr5:74169609-74169610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368661029	chr5:74169617-74169618	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190818790	chr5:74169620-74169621	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552470316	chr5:74169624-74169625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371611959	chr5:74169630-74169631	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371060212	chr5:74169633-74169634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183331874	chr5:74169655-74169656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561953702	chr5:74169663-74169664	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs115315582	chr5:74169664-74169665	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141419410	chr5:74169743-74169744	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571087234	chr5:74169757-74169758	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374149229	chr5:74169798-74169799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74729216	chr5:74169805-74169806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570832143	chr5:74169826-74169827	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187350164	chr5:74169837-74169838	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs568946684	chr5:74169860-74169861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201085362	chr5:74169915-74169916	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537945358	chr5:74169941-74169942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554767973	chr5:74169950-74169951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568255329	chr5:74169979-74169980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190936771	chr5:74170207-74170208	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs386689110	chr5:74170222-74170223	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs377401007	chr5:74170233-74170234	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554016708	chr5:74170299-74170300	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Amyotrophic lateral sclerosis	20685689	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74164800-74172000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:74165400-74172200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:74168200-74171800	Enhancers	HepG2	liver
4	chr5:74169200-74169400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr5:74169400-74173000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:74171800-74172600	Flanking Active TSS	HepG2	liver
7	chr5:74171800-74174800	Enhancers	Liver	Liver
8	chr5:74172000-74172600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:74172000-74172600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:74172000-74173800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:74172200-74172400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr5:74172200-74172400	Enhancers	Brain Cingulate Gyrus	brain
13	chr5:74172200-74172400	Enhancers	Brain Hippocampus Middle	brain
14	chr5:74172200-74172400	Enhancers	Brain Substantia Nigra	brain
15	chr5:74172200-74172600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:74172200-74172600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr5:74172200-74172600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:74172200-74172600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr5:74172200-74172600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr5:74172200-74172600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:74172200-74173800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr5:74172200-74174000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr5:74172400-74173200	Enhancers	Brain Anterior Caudate	brain
24	chr5:74172400-74173200	Weak transcription	Brain Hippocampus Middle	brain
25	chr5:74172400-74173400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr5:74172400-74173400	Weak transcription	Brain Substantia Nigra	brain
27	chr5:74172400-74173800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:74172400-74173800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr5:74172400-74174000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:74172600-74173000	Enhancers	HepG2	liver
31	chr5:74172600-74173600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:74172600-74173600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:74172600-74173600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:74172600-74173600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:74172600-74173600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr5:74172600-74173600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr5:74172600-74173600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:74172600-74179200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr5:74173000-74173600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:74173000-74173800	Enhancers	Brain Germinal Matrix	brain
41	chr5:74173000-74174000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr5:74173000-74174400	Flanking Active TSS	HepG2	liver
43	chr5:74173200-74174000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:74173200-74174400	Weak transcription	Brain Anterior Caudate	brain
45	chr5:74173200-74174600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr5:74173200-74174800	Enhancers	Brain Hippocampus Middle	brain
47	chr5:74173400-74173800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:74173400-74174600	Enhancers	Brain Cingulate Gyrus	brain
49	chr5:74173400-74175200	Enhancers	Brain Substantia Nigra	brain
50	chr5:74173600-74173800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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