Variant report

Variant	nsv916422
Chromosome Location	chr4:84965304-85145657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:656)
CpG islands
(count:489)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:84971074-84971640	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:84972221-84972448	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:84971021-84971585	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:85067531-85067809	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:84971193-84971437	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:85067585-85067821	GM12878	blood:	n/a	n/a
7	CBX3	chr4:85088813-85089099	HCT-116	colon:	n/a	n/a
8	CEBPB	chr4:85135957-85136188	A549	lung:	n/a	n/a
9	CEBPB	chr4:84984925-84985048	Hela-S3	cervix:	n/a	chr4:84984937-84984948 chr4:84984939-84984950
10	CEBPB	chr4:85017500-85017839	HepG2	liver:	n/a	chr4:85017666-85017677
11	CEBPB	chr4:85119744-85120069	IMR90	lung:	n/a	chr4:85119904-85119915
12	CEBPB	chr4:85057686-85057780	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:85079965-85080234	A549	lung:	n/a	n/a
14	CEBPB	chr4:84984801-84985070	H1-hESC	embryonic stem cell:	n/a	chr4:84984937-84984948 chr4:84984939-84984950
15	CEBPB	chr4:85080088-85080249	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:84984799-84985081	HepG2	liver:	n/a	chr4:84984937-84984948 chr4:84984939-84984950
17	CEBPB	chr4:85084572-85084750	HepG2	liver:	n/a	chr4:85084721-85084730 chr4:85084719-85084730
18	CEBPB	chr4:84984881-84984989	K562	blood:	n/a	chr4:84984937-84984948 chr4:84984939-84984950
19	CEBPB	chr4:85079993-85080193	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:85108449-85108714	H1-hESC	embryonic stem cell:	n/a	chr4:85108566-85108577
21	CEBPB	chr4:85108520-85108554	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:85119769-85120419	A549	lung:	n/a	chr4:85119904-85119915
23	CEBPB	chr4:85017568-85017768	K562	blood:	n/a	chr4:85017666-85017677
24	CEBPB	chr4:85017533-85017825	IMR90	lung:	n/a	chr4:85017666-85017677
25	CEBPB	chr4:85014175-85014209	HepG2	liver:	n/a	chr4:85014190-85014201 chr4:85014188-85014201 chr4:85014188-85014199
26	CEBPB	chr4:85119744-85120477	HepG2	liver:	n/a	chr4:85119904-85119915
27	CEBPB	chr4:85135969-85136221	HepG2	liver:	n/a	n/a
28	CHD2	chr4:84972781-84973067	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr4:85080957-85081224	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:85081080-85081230	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr4:85088780-85088930	GM12868	blood:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
32	CTCF	chr4:85072823-85073006	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr4:85088890-85089002	GM19240	blood:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
34	CTCF	chr4:85088780-85088930	HMEC	breast:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
35	CTCF	chr4:85081024-85081286	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:85081060-85081210	BE2_C	brain:	n/a	n/a
37	CTCF	chr4:85088840-85088990	AG04449	skin:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
38	CTCF	chr4:85072820-85072970	GM12873	blood:	n/a	n/a
39	CTCF	chr4:85072840-85072935	Fibrobl	skin:	n/a	n/a
40	CTCF	chr4:85088836-85089019	HepG2	liver:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
41	CTCF	chr4:85081040-85081190	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr4:85072680-85072830	RPTEC	kidney:	n/a	n/a
43	CTCF	chr4:85088850-85089010	Gliobla	brain:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
44	CTCF	chr4:85072820-85072970	GM12864	blood:	n/a	n/a
45	CTCF	chr4:85072817-85072980	GM19238	blood:	n/a	n/a
46	CTCF	chr4:85081080-85081230	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:85072820-85072970	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:85007280-85007430	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:85088820-85088970	GM06990	blood:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
50	CTCF	chr4:85088880-85089030	NHEK	skin:	n/a	chr4:85088908-85088924 chr4:85088907-85088925

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85145324-85145374	AG04449	skin:	fetal
2	chr4:85145324-85145374	AG04449	skin:	fetal
3	chr4:84991657-84991707	NH-A	brain:	n/a
4	chr4:84991657-84991707	PFSK-1	brain:	n/a
5	chr4:85048240-85048290	SK-N-SH_RA	brain:	n/a
6	chr4:84972436-84972486	HRE	kidney:	n/a
7	chr4:84991657-84991707	HRCEpiC	kidney:	n/a
8	chr4:85076551-85076601	GM06990	blood:	n/a
9	chr4:85020829-85020879	AG09319	gingival:	n/a
10	chr4:85020829-85020879	U87	brain:	n/a
11	chr4:85139232-85139282	GM06990	blood:	n/a
12	chr4:85145324-85145374	GM12891	blood:	n/a
13	chr4:84979076-84979126	HCM	heart:	n/a
14	chr4:85139232-85139282	Hepatocyte	liver:	n/a
15	chr4:84991657-84991707	HAEpiC	amniotic membrane:	n/a
16	chr4:84979076-84979126	ProgFib	skin:	n/a
17	chr4:84979076-84979126	GM12892	blood:	n/a
18	chr4:85139232-85139282	AG10803	skin:	n/a
19	chr4:85020829-85020879	HCM	heart:	n/a
20	chr4:85076551-85076601	NH-A	brain:	n/a
21	chr4:84979076-84979126	Caco-2	colon:	n/a
22	chr4:84979076-84979126	AG09309	skin:	n/a
23	chr4:84972436-84972486	HCM	heart:	n/a
24	chr4:84972436-84972486	GM12878	blood:	n/a
25	chr4:85020829-85020879	HepG2	liver:	n/a
26	chr4:85020829-85020879	ECC-1	luminal epithelium:	n/a
27	chr4:85145324-85145374	GM19239	blood:	n/a
28	chr4:85020829-85020879	SK-N-MC	brain:	n/a
29	chr4:84991657-84991707	HCT-116	colon:	n/a
30	chr4:85145324-85145374	Hepatocyte	liver:	n/a
31	chr4:84991657-84991707	HNPCEpiC	eye:	n/a
32	chr4:84979076-84979126	RPTEC	kidney:	n/a
33	chr4:85145324-85145374	HCM	heart:	n/a
34	chr4:85020829-85020879	BE2_C	brain:	n/a
35	chr4:85139232-85139282	LNCaP	prostate:	n/a
36	chr4:84979076-84979126	HCPEpiC	choroid plexus:	n/a
37	chr4:85139232-85139282	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:84991657-84991707	SKMC	muscle:	n/a
39	chr4:85076551-85076601	HCF	heart:	n/a
40	chr4:85048240-85048290	Hepatocyte	liver:	n/a
41	chr4:85076551-85076601	HCM	heart:	n/a
42	chr4:85145324-85145374	PFSK-1	brain:	n/a
43	chr4:85048240-85048290	HEEpiC	esophagus:	n/a
44	chr4:85139232-85139282	HMEC	breast:	n/a
45	chr4:85048240-85048290	Jurkat	blood:	n/a
46	chr4:85076551-85076601	NHBE	bronchial:	n/a
47	chr4:85145324-85145374	AG09309	skin:	n/a
48	chr4:84972436-84972486	HNPCEpiC	eye:	n/a
49	chr4:84991657-84991707	GM06990	blood:	n/a
50	chr4:85076551-85076601	PrEC	prostate:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:84827046..84827675-chr4:85088517..85089246,2	MCF-7	breast:
2	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
3	chr20:52481552..52482195-chr4:85078491..85079377,2	MCF-7	breast:
4	chr4:84969530..84971109-chr4:84977042..84979357,2	K562	blood:
5	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
6	chr4:85080701..85081585-chr4:85425136..85425979,2	MCF-7	breast:
7	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
8	chr4:85072631..85073368-chr4:85450368..85450912,2	MCF-7	breast:
9	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
10	chr4:84967010..84969386-chr4:84969722..84972358,2	MCF-7	breast:
11	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
12	chr4:84972192..84974341-chr4:84974515..84976021,2	K562	blood:
13	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
14	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
15	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
16	chr4:84967010..84969386-chr4:84969722..84972358,2	MCF-7	breast:
17	chr4:84565617..84566470-chr4:85088713..85089282,2	MCF-7	breast:
18	chr4:84969530..84971109-chr4:84977042..84979357,2	K562	blood:
19	chr4:84882460..84883415-chr4:85088632..85089152,2	MCF-7	breast:
20	chr4:85072431..85073209-chr4:85424476..85425190,3	MCF-7	breast:
21	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
22	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
23	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
24	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
25	chr4:84972192..84974341-chr4:84974515..84976021,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKX6-1-2	chr4:85070372-85070409	ENSG00000250546
2	lnc-NKX6-1-2	chr4:85069200-85069283	ENSG00000250546
3	lnc-NKX6-1-2	chr4:85068886-85069283	ENSG00000250546
4	lnc-NKX6-1-3	chr4:85075800-85075907	ucscGeneNc_uc010ikd_1
5	lnc-NKX6-1-2	chr4:85070372-85070441	ENSG00000250546

No data

Variant related genes	Relation type
ENSG00000250546	TF binding region
ENSG00000250546	CpG island
F3	miRNA target sites
USP25	miRNA target sites
VAMP2	miRNA target sites
FOXP1	miRNA target sites

Extended variants
information (count: 2625 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2625 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567860898	chr4:84970215-84970216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552445742	chr4:84970222-84970223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371425171	chr4:84970240-84970241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557038956	chr4:84970269-84970270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148873884	chr4:84970277-84970278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570515798	chr4:84970278-84970279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374329108	chr4:84970284-84970285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557369286	chr4:84970336-84970337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77850354	chr4:84970399-84970400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540137854	chr4:84970404-84970405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143575338	chr4:84970414-84970415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573794733	chr4:84970415-84970416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544106419	chr4:84970424-84970425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562985304	chr4:84970473-84970474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76368497	chr4:84970489-84970490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545418683	chr4:84970494-84970495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201932685	chr4:84970507-84970508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560491633	chr4:84970510-84970511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185005567	chr4:84970530-84970531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562059771	chr4:84970556-84970557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567728491	chr4:84970566-84970567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528015624	chr4:84970571-84970572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112758638	chr4:84970603-84970604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550140824	chr4:84970692-84970693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189171168	chr4:84970697-84970698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541306855	chr4:84970717-84970718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564190092	chr4:84970722-84970723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539193738	chr4:84970724-84970725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557283252	chr4:84970736-84970737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181063251	chr4:84970756-84970757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185956066	chr4:84970772-84970773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374129702	chr4:84970794-84970795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536020366	chr4:84970798-84970799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555220963	chr4:84970831-84970832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201433101	chr4:84970837-84970838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369288044	chr4:84970838-84970839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573886356	chr4:84970866-84970867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs60804318	chr4:84970867-84970868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371663372	chr4:84970893-84970894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533353717	chr4:84970898-84970899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528275457	chr4:84970900-84970901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1921871	chr4:84970969-84970970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556131652	chr4:84971001-84971002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114366095	chr4:84971017-84971018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80214907	chr4:84971081-84971082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189208999	chr4:84971082-84971083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527711215	chr4:84971135-84971136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543070187	chr4:84971187-84971188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561608764	chr4:84971221-84971222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529091764	chr4:84971266-84971267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:84970200-84970400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:84970400-84971400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:84970400-84971600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr4:84970600-84970800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr4:84970600-84970800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:84970600-84973800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:84970800-84971400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:84970800-84973800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:84970800-84973800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:84970800-84973800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr4:84971000-84973600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:84971000-84973800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:84971200-84973400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:84971200-84973600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr4:84971200-84973600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:84971400-84972600	Enhancers	Fetal Muscle Leg	muscle
17	chr4:84971400-84973400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:84971400-84973400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:84971400-84973800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:84971400-84973800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:84971600-84972200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:84971600-84973600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:84971800-84972000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:84971800-84973400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:84972000-84972800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:84972800-84973000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr4:84973000-84974200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:84973400-84974600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr4:84973600-84973800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:84973600-84979000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:84973800-84979000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:84973800-84979200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr4:84973800-84979200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:84973800-84979200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:84973800-84979200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr4:84973800-84979200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:84973800-84979200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:84973800-84980200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:84974800-84975000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:84974800-84975000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:84978000-84979000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr4:84978600-84979800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:84979000-84979600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:84979000-84979600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:84979000-84979800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:84979000-84980400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:84979200-84979600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr4:84979200-84979600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:84979200-84979800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:84979200-84979800	Enhancers	HUES48 Cell Line	embryonic stem cell

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