Variant report

Variant	nsv10412
Chromosome Location	chr4:649291-651178
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:550)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:649384-649973	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:649464-649688	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:649734-649735	K562	blood:	n/a	n/a
4	E2F6	chr4:649783-649934	K562	blood:	n/a	n/a
5	EGR1	chr4:649323-649512	K562	blood:	n/a	n/a
6	EP300	chr4:649728-649758	HepG2	liver:	n/a	n/a
7	GABPA	chr4:650957-651226	K562	blood:	n/a	n/a
8	MAFF	chr4:649761-649812	HepG2	liver:	n/a	n/a
9	MAX	chr4:649476-649681	K562	blood:	n/a	n/a
10	MAX	chr4:649648-649796	HepG2	liver:	n/a	n/a
11	MAX	chr4:648843-650038	HepG2	liver:	n/a	chr4:649898-649905
12	MAZ	chr4:649743-649943	HepG2	liver:	n/a	chr4:649898-649905
13	NR2F2	chr4:651086-652523	MCF-7	breast:	n/a	n/a
14	NR2F2	chr4:651092-652404	K562	blood:	n/a	n/a
15	NR2F2	chr4:651141-652387	K562	blood:	n/a	n/a
16	POLR2A	chr4:651059-651923	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr4:649955-649970	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr4:651168-651870	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr4:650478-650937	K562	blood:	n/a	n/a
20	POLR2A	chr4:649476-649808	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr4:651163-652297	K562	blood:	n/a	n/a
22	POLR2A	chr4:649826-649920	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr4:650003-650018	H1-hESC	embryonic stem cell:	n/a	n/a
24	RXRA	chr4:651081-652578	HepG2	liver:	n/a	chr4:652317-652333
25	RXRA	chr4:651060-652413	H1-hESC	embryonic stem cell:	n/a	chr4:652317-652333
26	RXRA	chr4:651082-652423	H1-hESC	embryonic stem cell:	n/a	chr4:652317-652333
27	ZBTB7A	chr4:649389-649547	HepG2	liver:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:650457-650507	GM19239	blood:	n/a
2	chr4:650457-650507	GM19239	blood:	n/a
3	chr4:649901-649951	HCPEpiC	choroid plexus:	n/a
4	chr4:649540-649590	ovcar-3	ovarian:	n/a
5	chr4:649901-649951	BJ	skin:	n/a
6	chr4:651113-651163	HepG2	liver:	n/a
7	chr4:649901-649951	PrEC	prostate:	n/a
8	chr4:649503-649553	HRPEpiC	eye:	n/a
9	chr4:649881-649931	GM19239	blood:	n/a
10	chr4:649503-649553	SKMC	muscle:	n/a
11	chr4:649540-649590	T-47D	breast:	n/a
12	chr4:650632-650682	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:649881-649931	HEEpiC	esophagus:	n/a
14	chr4:649573-649623	PANC-1	pancreas:	n/a
15	chr4:651113-651163	H1-hESC	embryonic stem cell:	embryo
16	chr4:650632-650682	U87	brain:	n/a
17	chr4:649881-649931	BJ	skin:	n/a
18	chr4:649901-649951	HIPEpiC	eye:	n/a
19	chr4:649901-649951	AoSMC	blood vessel:	n/a
20	chr4:649503-649553	NHBE	bronchial:	n/a
21	chr4:650632-650682	SK-N-SH	brain:	n/a
22	chr4:649573-649623	LNCaP	prostate:	n/a
23	chr4:650632-650682	PrEC	prostate:	n/a
24	chr4:651113-651163	AG09309	skin:	n/a
25	chr4:649845-649895	ovcar-3	ovarian:	n/a
26	chr4:650457-650507	PrEC	prostate:	n/a
27	chr4:649573-649623	MCF-7	breast:	n/a
28	chr4:649540-649590	NHBE	bronchial:	n/a
29	chr4:650457-650507	MCF-7	breast:	n/a
30	chr4:649845-649895	Hepatocyte	liver:	n/a
31	chr4:649901-649951	HL-60	blood:	n/a
32	chr4:649901-649951	AG04450	lung:	fetal
33	chr4:651113-651163	SK-N-MC	brain:	n/a
34	chr4:649573-649623	RPTEC	kidney:	n/a
35	chr4:649901-649951	NH-A	brain:	n/a
36	chr4:650457-650507	SK-N-SH_RA	brain:	n/a
37	chr4:649845-649895	GM12892	blood:	n/a
38	chr4:651113-651163	IMR90	lung:	fetal
39	chr4:651113-651163	MCF10A-Er-Src	breast:	n/a
40	chr4:649901-649951	NHBE	bronchial:	n/a
41	chr4:649901-649951	NT2-D1	testis:	n/a
42	chr4:650457-650507	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:649901-649951	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:649503-649553	PFSK-1	brain:	n/a
45	chr4:650457-650507	GM12878	blood:	n/a
46	chr4:649845-649895	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:649540-649590	MCF-7	breast:	n/a
48	chr4:650457-650507	HAEpiC	amniotic membrane:	n/a
49	chr4:649540-649590	PrEC	prostate:	n/a
50	chr4:651113-651163	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr4:642131..644821-chr4:649750..652284,2	MCF-7	breast:
2	chr4:649938..652851-chr4:653641..657433,6	K562	blood:
3	chr4:644808..646339-chr4:648173..650037,2	K562	blood:
4	chr4:644162..647846-chr4:649268..652076,4	MCF-7	breast:
5	chr4:613849..616261-chr4:650426..653017,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5I-1	chr4:648871-649434	ENSG00000242686.1

No data

Variant related genes	Relation type
ENSG00000242686	TF binding region
ENSG00000242686	CpG island
ENSG00000272927	chromatin interactions
ENSG00000242686	chromatin interactions
ENSG00000133256	chromatin interactions

Extended variants
information (count: 148 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:148 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570642883	chr4:649315-649316	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs563714346	chr4:649316-649317	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs114577486	chr4:649351-649352	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs73056598	chr4:649398-649399	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532956480	chr4:649422-649423	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs563327290	chr4:649442-649443	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143316218	chr4:649480-649481	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546488529	chr4:649482-649483	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564865925	chr4:649500-649501	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531967210	chr4:649506-649507	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs183694221	chr4:649514-649515	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568857091	chr4:649536-649537	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535921693	chr4:649540-649541	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548306480	chr4:649564-649565	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567855892	chr4:649582-649583	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs28535694	chr4:649597-649598	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553686700	chr4:649613-649614	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs578240946	chr4:649614-649615	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs377387981	chr4:649622-649623	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs28742899	chr4:649639-649640	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs371553443	chr4:649678-649679	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372732725	chr4:649679-649680	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115328178	chr4:649680-649681	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs199533451	chr4:649692-649693	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377201145	chr4:649693-649694	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572681474	chr4:649696-649697	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374725416	chr4:649711-649712	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs138955314	chr4:649734-649735	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370605672	chr4:649741-649742	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368173258	chr4:649763-649764	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201953373	chr4:649785-649786	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112918073	chr4:649804-649805	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377101351	chr4:649805-649806	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376576406	chr4:649814-649815	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200993710	chr4:649820-649821	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372752579	chr4:649833-649834	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187600546	chr4:649846-649847	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528408885	chr4:649872-649873	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs28630797	chr4:649876-649877	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs566604978	chr4:649963-649964	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs533886335	chr4:649969-649970	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs547185588	chr4:649970-649971	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs143150302	chr4:649990-649991	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369121532	chr4:649995-649996	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs192530891	chr4:650012-650013	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs377140204	chr4:650013-650014	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs147482093	chr4:650021-650022	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376325785	chr4:650044-650045	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs142802752	chr4:650057-650058	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs150360174	chr4:650063-650064	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:631400-657000	Weak transcription	Right Atrium	heart
2	chr4:641800-657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:642200-652800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:642400-654600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:642800-657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:643000-657000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:645800-649400	Weak transcription	Pancreas	Pancrea
8	chr4:645800-656800	Weak transcription	Gastric	stomach
9	chr4:646800-650600	Enhancers	Brain Angular Gyrus	brain
10	chr4:647000-650000	Enhancers	Brain Anterior Caudate	brain
11	chr4:647200-651200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr4:648400-650200	Enhancers	Brain Substantia Nigra	brain
13	chr4:648400-657000	Weak transcription	Right Ventricle	heart
14	chr4:648600-649600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:648600-650000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr4:648600-650600	Enhancers	Spleen	Spleen
17	chr4:648800-650000	Flanking Bivalent TSS/Enh	HepG2	liver
18	chr4:648800-650800	Enhancers	Brain Cingulate Gyrus	brain
19	chr4:648800-653400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:649000-649600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:649000-651000	Enhancers	Brain Hippocampus Middle	brain
22	chr4:649000-652800	Weak transcription	Brain Germinal Matrix	brain
23	chr4:649200-652800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr4:649200-653000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:649400-649800	ZNF genes & repeats	Pancreas	Pancrea
26	chr4:649400-650000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:649600-650000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:649600-650000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:649800-651000	Weak transcription	Pancreas	Pancrea
30	chr4:649800-653200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:649800-655600	Weak transcription	Thymus	Thymus
32	chr4:650000-650400	Weak transcription	Brain Anterior Caudate	brain
33	chr4:650000-650600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr4:650000-653200	Weak transcription	Fetal Brain Female	brain
35	chr4:650000-654000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:650000-654200	Enhancers	HepG2	liver
37	chr4:650200-651200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr4:650200-652800	Weak transcription	Brain Substantia Nigra	brain
39	chr4:650400-650600	Enhancers	Brain Anterior Caudate	brain
40	chr4:650400-651200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:650600-650800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr4:650600-651000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:650600-651200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:650600-651200	Weak transcription	Spleen	Spleen
45	chr4:650600-652600	Weak transcription	Brain Anterior Caudate	brain
46	chr4:650600-652800	Weak transcription	Brain Angular Gyrus	brain
47	chr4:650800-652800	Weak transcription	Primary T cells from cord blood	blood
48	chr4:650800-656000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr4:651000-651200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:651000-651200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle

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