Variant report

Variant	esv3343366
Chromosome Location	chr4:3441654-3443552
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	chr4:3443453-3443675	HepG2	liver:	n/a	n/a
2	CEBPD	chr4:3443344-3444000	HepG2	liver:	n/a	n/a
3	CHD2	chr4:3442759-3442777	HepG2	liver:	n/a	n/a
4	CHD2	chr4:3443379-3443859	HepG2	liver:	n/a	chr4:3443687-3443697
5	CTCF	chr4:3442660-3442810	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr4:3442727-3442795	NHEK	skin:	n/a	n/a
7	EBF1	chr4:3442128-3442222	GM12878	blood:	n/a	chr4:3442173-3442186 chr4:3442173-3442184 chr4:3442174-3442184 chr4:3442175-3442184
8	ELK1	chr4:3442808-3442820	K562	blood:	n/a	n/a
9	EP300	chr4:3443364-3443856	HepG2	liver:	n/a	n/a
10	FOS	chr4:3442688-3442938	MCF10A-Er-Src	breast:	n/a	chr4:3442784-3442794
11	HDAC2	chr4:3443401-3443863	HepG2	liver:	n/a	n/a
12	HEY1	chr4:3443381-3443880	HepG2	liver:	n/a	n/a
13	HEY1	chr4:3443305-3443967	HepG2	liver:	n/a	n/a
14	JUND	chr4:3443475-3443735	HepG2	liver:	n/a	chr4:3443692-3443701
15	MAFF	chr4:3442690-3442913	HepG2	liver:	n/a	chr4:3442782-3442796 chr4:3442776-3442794
16	MAFK	chr4:3443469-3443535	HepG2	liver:	n/a	n/a
17	MAFK	chr4:3442709-3442923	K562	blood:	n/a	chr4:3442783-3442792 chr4:3442778-3442793 chr4:3442782-3442796 chr4:3442785-3442795
18	MAFK	chr4:3442692-3442823	Hela-S3	cervix:	n/a	chr4:3442783-3442792 chr4:3442778-3442793 chr4:3442782-3442796 chr4:3442785-3442795
19	MAFK	chr4:3442661-3442884	IMR90	lung:	n/a	chr4:3442783-3442792 chr4:3442778-3442793 chr4:3442782-3442796 chr4:3442785-3442795
20	MAFK	chr4:3442657-3442817	HepG2	liver:	n/a	chr4:3442783-3442792 chr4:3442778-3442793 chr4:3442782-3442796 chr4:3442785-3442795
21	MAFK	chr4:3442685-3442928	HepG2	liver:	n/a	chr4:3442783-3442792 chr4:3442778-3442793 chr4:3442782-3442796 chr4:3442785-3442795
22	MAX	chr4:3443519-3443920	HepG2	liver:	n/a	n/a
23	MAX	chr4:3443155-3445641	HepG2	liver:	n/a	chr4:3445533-3445541 chr4:3443948-3443958 chr4:3445535-3445544 chr4:3445534-3445545 chr4:3445536-3445543 chr4:3445534-3445544
24	MAX	chr4:3443225-3445755	HepG2	liver:	n/a	chr4:3445533-3445541 chr4:3443948-3443958 chr4:3445535-3445544 chr4:3445534-3445545 chr4:3445536-3445543 chr4:3445534-3445544
25	MAZ	chr4:3442680-3442736	Hela-S3	cervix:	n/a	n/a
26	MAZ	chr4:3443220-3444465	HepG2	liver:	n/a	chr4:3443948-3443958
27	MXI1	chr4:3443266-3443853	HepG2	liver:	n/a	n/a
28	MYBL2	chr4:3443054-3444720	HepG2	liver:	n/a	n/a
29	MYBL2	chr4:3443382-3443862	HepG2	liver:	n/a	n/a
30	MYC	chr4:3443447-3443499	MCF10A-Er-Src	breast:	n/a	n/a
31	MYC	chr4:3442822-3442894	MCF10A-Er-Src	breast:	n/a	n/a
32	NFIC	chr4:3441687-3442242	ECC-1	luminal epithelium:	n/a	chr4:3441953-3441970 chr4:3441954-3441970
33	NFIC	chr4:3443238-3443872	HepG2	liver:	n/a	n/a
34	POLR2A	chr4:3441841-3442104	HepG2	liver:	n/a	n/a
35	POLR2A	chr4:3442671-3444054	HepG2	liver:	n/a	n/a
36	POLR2A	chr4:3443485-3443599	ProgFib	skin:	n/a	n/a
37	POLR2A	chr4:3443299-3444029	HepG2	liver:	n/a	n/a
38	POLR2A	chr4:3442149-3442156	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr4:3442676-3445578	HepG2	liver:	n/a	n/a
40	POLR2A	chr4:3443499-3445533	HepG2	liver:	n/a	n/a
41	POLR2A	chr4:3443407-3443866	HepG2	liver:	n/a	n/a
42	POLR2A	chr4:3442235-3442370	HepG2	liver:	n/a	n/a
43	POLR2A	chr4:3442639-3442781	HepG2	liver:	n/a	n/a
44	POLR2A	chr4:3443293-3443917	HepG2	liver:	n/a	n/a
45	POLR2A	chr4:3443351-3443893	HepG2	liver:	n/a	n/a
46	POLR2A	chr4:3443257-3443964	HepG2	liver:	n/a	n/a
47	POLR2A	chr4:3442707-3442827	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr4:3441987-3442140	HepG2	liver:	n/a	n/a
49	RCOR1	chr4:3443269-3443520	K562	blood:	n/a	n/a
50	RCOR1	chr4:3442766-3443037	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3442962-3443012	H1-hESC	embryonic stem cell:	embryo
2	chr4:3442962-3443012	H1-hESC	embryonic stem cell:	embryo
3	chr4:3443025-3443075	Caco-2	colon:	n/a
4	chr4:3442962-3443012	HCT-116	colon:	n/a
5	chr4:3442311-3442361	SK-N-MC	brain:	n/a
6	chr4:3442962-3443012	RPTEC	kidney:	n/a
7	chr4:3442311-3442361	NH-A	brain:	n/a
8	chr4:3442311-3442361	ovcar-3	ovarian:	n/a
9	chr4:3442311-3442361	MCF10A-Er-Src	breast:	n/a
10	chr4:3442962-3443012	U87	brain:	n/a
11	chr4:3442962-3443012	HCM	heart:	n/a
12	chr4:3442962-3443012	HIPEpiC	eye:	n/a
13	chr4:3442962-3443012	BJ	skin:	n/a
14	chr4:3442962-3443012	GM12878	blood:	n/a
15	chr4:3442311-3442361	ProgFib	skin:	n/a
16	chr4:3442311-3442361	MCF-7	breast:	n/a
17	chr4:3442311-3442361	HRPEpiC	eye:	n/a
18	chr4:3443025-3443075	HRE	kidney:	n/a
19	chr4:3442311-3442361	PANC-1	pancreas:	n/a
20	chr4:3442962-3443012	PrEC	prostate:	n/a
21	chr4:3443025-3443075	BJ	skin:	n/a
22	chr4:3442962-3443012	K562	blood:	n/a
23	chr4:3442311-3442361	HRE	kidney:	n/a
24	chr4:3442311-3442361	K562	blood:	n/a
25	chr4:3442311-3442361	NHDF-neo	bronchial:	n/a
26	chr4:3442311-3442361	HCT-116	colon:	n/a
27	chr4:3443025-3443075	K562	blood:	n/a
28	chr4:3442962-3443012	HNPCEpiC	eye:	n/a
29	chr4:3442311-3442361	HCF	heart:	n/a
30	chr4:3443025-3443075	HCPEpiC	choroid plexus:	n/a
31	chr4:3443025-3443075	CMK	blood:	n/a
32	chr4:3443025-3443075	GM19239	blood:	n/a
33	chr4:3442311-3442361	AG04449	skin:	fetal
34	chr4:3442311-3442361	HMEC	breast:	n/a
35	chr4:3443025-3443075	ECC-1	luminal epithelium:	n/a
36	chr4:3442962-3443012	NT2-D1	testis:	n/a
37	chr4:3443025-3443075	U87	brain:	n/a
38	chr4:3442962-3443012	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:3442311-3442361	T-47D	breast:	n/a
40	chr4:3442962-3443012	AG10803	skin:	n/a
41	chr4:3442311-3442361	HUVEC	blood vessel:	n/a
42	chr4:3442311-3442361	AG09309	skin:	n/a
43	chr4:3443025-3443075	HCT-116	colon:	n/a
44	chr4:3443025-3443075	AG09309	skin:	n/a
45	chr4:3442962-3443012	GM19239	blood:	n/a
46	chr4:3443025-3443075	LNCaP	prostate:	n/a
47	chr4:3442962-3443012	HEK293	kidney:	embryo
48	chr4:3442962-3443012	SK-N-SH	brain:	n/a
49	chr4:3442962-3443012	PFSK-1	brain:	n/a
50	chr4:3442311-3442361	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3416652..3419915-chr4:3441173..3444245,3	MCF-7	breast:
2	chr4:3387900..3390200-chr4:3439176..3442077,2	MCF-7	breast:
3	chr12:52607035..52609334-chr4:3440706..3442862,2	MCF-7	breast:
4	chr4:3347550..3348452-chr4:3441019..3441869,2	K562	blood:
5	chr4:3428890..3430804-chr4:3441748..3443973,2	MCF-7	breast:
6	chr4:3439130..3442230-chr4:3483136..3486025,3	MCF-7	breast:
7	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
8	chr4:3297878..3299647-chr4:3439847..3442316,2	MCF-7	breast:

Variant related genes	Relation type
HGFAC	TF binding region
HGFAC	CpG island
ENSG00000159788	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571911655	chr4:3441669-3441670	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs560541300	chr4:3441670-3441671	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs75330267	chr4:3441687-3441688	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577857457	chr4:3441696-3441697	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544018443	chr4:3441732-3441733	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563828600	chr4:3441733-3441734	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182779234	chr4:3441740-3441741	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572429422	chr4:3441753-3441754	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187489562	chr4:3441843-3441844	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528455116	chr4:3441848-3441849	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs556061037	chr4:3441849-3441850	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571398116	chr4:3441856-3441857	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530873795	chr4:3441863-3441864	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs550663325	chr4:3441912-3441913	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs190985147	chr4:3441929-3441930	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535653972	chr4:3441970-3441971	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555355862	chr4:3441977-3441978	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs114254914	chr4:3441988-3441989	Genic enhancers Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs762861	chr4:3442011-3442012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs183074704	chr4:3442029-3442030	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs577717685	chr4:3442031-3442032	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529236969	chr4:3442057-3442058	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115911722	chr4:3442058-3442059	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs874418	chr4:3442069-3442070	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574270632	chr4:3442072-3442073	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368725047	chr4:3442098-3442099	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187510142	chr4:3442116-3442117	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs762862	chr4:3442146-3442147	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375711720	chr4:3442193-3442194	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545526062	chr4:3442223-3442224	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545387616	chr4:3442225-3442226	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564888514	chr4:3442232-3442233	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs73193400	chr4:3442259-3442260	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs550624631	chr4:3442263-3442264	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs567453888	chr4:3442328-3442329	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191697206	chr4:3442398-3442399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529054957	chr4:3442405-3442406	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549205027	chr4:3442408-3442409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565824489	chr4:3442410-3442411	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56379800	chr4:3442414-3442415	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192080705	chr4:3442429-3442430	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546903183	chr4:3442448-3442449	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555174274	chr4:3442501-3442502	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558108923	chr4:3442529-3442530	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142667333	chr4:3442540-3442541	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116772679	chr4:3442550-3442551	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76758203	chr4:3442572-3442573	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184882913	chr4:3442590-3442591	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73193402	chr4:3442630-3442631	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs115513037	chr4:3442638-3442639	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3417200-3444800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:3419200-3444600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr4:3427000-3442000	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:3427000-3443200	Weak transcription	Brain Substantia Nigra	brain
5	chr4:3430800-3445200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr4:3431600-3442600	Weak transcription	Colonic Mucosa	Colon
7	chr4:3431800-3444600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr4:3433000-3445200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr4:3433200-3444800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:3433600-3444600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:3434200-3442600	Weak transcription	Liver	Liver
12	chr4:3436400-3441800	Weak transcription	Lung	lung
13	chr4:3436400-3443000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr4:3436400-3444400	Weak transcription	Primary T cells from cord blood	blood
15	chr4:3436400-3444400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:3436400-3445200	Weak transcription	Fetal Intestine Small	intestine
17	chr4:3436600-3449000	Weak transcription	Fetal Brain Female	brain
18	chr4:3436800-3443000	Enhancers	Fetal Muscle Leg	muscle
19	chr4:3436800-3445400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:3437000-3442600	Enhancers	Fetal Muscle Trunk	muscle
21	chr4:3437000-3450000	Weak transcription	Brain Germinal Matrix	brain
22	chr4:3437200-3451200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:3437800-3443000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:3438000-3448000	Weak transcription	Right Ventricle	heart
25	chr4:3438600-3444800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:3438800-3445400	Weak transcription	Gastric	stomach
27	chr4:3439000-3445400	Weak transcription	Pancreas	Pancrea
28	chr4:3439200-3445400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr4:3439400-3442600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:3439400-3442600	Weak transcription	NH-A	brain
31	chr4:3439400-3442800	Weak transcription	Osteobl	bone
32	chr4:3439600-3442600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:3440000-3441800	Weak transcription	HMEC	breast
34	chr4:3440000-3442800	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr4:3440400-3442600	Weak transcription	Esophagus	oesophagus
36	chr4:3440400-3445200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr4:3440600-3442600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:3441000-3441800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:3441000-3441800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:3441000-3443200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:3441200-3441800	Enhancers	Spleen	Spleen
42	chr4:3441200-3442000	ZNF genes & repeats	Fetal Stomach	stomach
43	chr4:3441400-3442000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:3441400-3442200	Enhancers	Brain Hippocampus Middle	brain
45	chr4:3441400-3443200	Enhancers	Fetal Lung	lung
46	chr4:3441400-3443800	Enhancers	A549	lung
47	chr4:3441600-3441800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr4:3441600-3442200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:3441600-3442800	Enhancers	HepG2	liver
50	chr4:3441600-3443200	Enhancers	NHEK	skin

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