Variant report

Variant	esv1007958
Chromosome Location	chr4:2904137-2914601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:183)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:2912295-2912379	Fibrobl	skin:	n/a	n/a
2	CTCF	chr4:2912180-2912330	BJ	skin:	n/a	n/a
3	CTCF	chr4:2912305-2912373	GM13977	blood:	n/a	n/a
4	CTCF	chr4:2912254-2912403	GM20000	blood:	n/a	n/a
5	CTCF	chr4:2912300-2912450	HRE	kidney:	n/a	n/a
6	CTCF	chr4:2912209-2912425	HepG2	liver:	n/a	n/a
7	CTCF	chr4:2912260-2912410	GM12873	blood:	n/a	n/a
8	CTCF	chr4:2912242-2912447	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:2912220-2912370	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr4:2912234-2912442	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:2912300-2912450	RPTEC	kidney:	n/a	n/a
12	CTCF	chr4:2912220-2912370	HCFaa	heart:	n/a	n/a
13	CTCF	chr4:2912280-2912430	RPTEC	kidney:	n/a	n/a
14	CTCF	chr4:2912320-2912470	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr4:2912340-2912490	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr4:2912291-2912393	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr4:2912300-2912450	GM12871	blood:	n/a	n/a
18	CTCF	chr4:2912170-2912497	K562	blood:	n/a	n/a
19	CTCF	chr4:2911544-2911678	Hela-S3	cervix:	n/a	chr4:2911597-2911613 chr4:2911598-2911619
20	CTCF	chr4:2912234-2912440	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr4:2912514-2912520	GM19239	blood:	n/a	n/a
22	CTCF	chr4:2912220-2912370	GM12865	blood:	n/a	n/a
23	CTCF	chr4:2911558-2911597	GM12878	blood:	n/a	n/a
24	CTCF	chr4:2912260-2912410	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr4:2912280-2912430	AG10803	skin:	n/a	n/a
26	CTCF	chr4:2912220-2912370	HPF	lung:	n/a	n/a
27	CTCF	chr4:2912227-2912482	GM12891	blood:	n/a	n/a
28	CTCF	chr4:2912262-2912403	GM10248	blood:	n/a	n/a
29	CTCF	chr4:2912200-2912350	HepG2	liver:	n/a	n/a
30	CTCF	chr4:2912240-2912390	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr4:2912260-2912410	AG09309	skin:	n/a	n/a
32	CTCF	chr4:2912300-2912450	NB4	blood:	n/a	n/a
33	CTCF	chr4:2912220-2912370	HMF	breast:	n/a	n/a
34	CTCF	chr4:2912340-2912490	HAc	cerebellar:	n/a	n/a
35	CTCF	chr4:2912231-2912525	K562	blood:	n/a	n/a
36	CTCF	chr4:2912300-2912450	HMF	breast:	n/a	n/a
37	CTCF	chr4:2912271-2912409	HepG2	liver:	n/a	n/a
38	CTCF	chr4:2912220-2912370	BJ	skin:	n/a	n/a
39	CTCF	chr4:2911532-2911666	HepG2	liver:	n/a	chr4:2911597-2911613 chr4:2911598-2911619
40	CTCF	chr4:2912240-2912390	AG04450	lung:	n/a	n/a
41	CTCF	chr4:2912260-2912410	SAEC	small airway:	n/a	n/a
42	CTCF	chr4:2912220-2912370	GM12873	blood:	n/a	n/a
43	CTCF	chr4:2911280-2911430	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:2911960-2912110	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:2912300-2912450	GM12864	blood:	n/a	n/a
46	CTCF	chr4:2912720-2912870	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr4:2912240-2912390	AG04449	skin:	n/a	n/a
48	CTCF	chr4:2912251-2912435	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:2912260-2912410	K562	blood:	n/a	n/a
50	CTCF	chr4:2912260-2912410	HRPEpiC	eye:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2906691-2906741	NB4	blood:	n/a
2	chr4:2906870-2906920	PANC-1	pancreas:	n/a
3	chr4:2906769-2906819	SKMC	muscle:	n/a
4	chr4:2906769-2906819	HRPEpiC	eye:	n/a
5	chr4:2906691-2906741	HEK293	kidney:	embryo
6	chr4:2906870-2906920	HAEpiC	amniotic membrane:	n/a
7	chr4:2906691-2906741	AoSMC	blood vessel:	n/a
8	chr4:2906870-2906920	Hepatocyte	liver:	n/a
9	chr4:2906691-2906741	GM06990	blood:	n/a
10	chr4:2906870-2906920	HCPEpiC	choroid plexus:	n/a
11	chr4:2906769-2906819	RPTEC	kidney:	n/a
12	chr4:2906870-2906920	HUVEC	blood vessel:	n/a
13	chr4:2906691-2906741	GM12892	blood:	n/a
14	chr4:2906769-2906819	PrEC	prostate:	n/a
15	chr4:2906870-2906920	HEEpiC	esophagus:	n/a
16	chr4:2906870-2906920	HEK293	kidney:	embryo
17	chr4:2906691-2906741	SK-N-SH	brain:	n/a
18	chr4:2906870-2906920	NB4	blood:	n/a
19	chr4:2906769-2906819	MCF-7	breast:	n/a
20	chr4:2906691-2906741	SK-N-SH_RA	brain:	n/a
21	chr4:2906691-2906741	SK-N-MC	brain:	n/a
22	chr4:2906691-2906741	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:2906691-2906741	Hela-S3	cervix:	n/a
24	chr4:2906870-2906920	HCT-116	colon:	n/a
25	chr4:2906870-2906920	GM12892	blood:	n/a
26	chr4:2906870-2906920	Caco-2	colon:	n/a
27	chr4:2906691-2906741	Caco-2	colon:	n/a
28	chr4:2906769-2906819	HIPEpiC	eye:	n/a
29	chr4:2906691-2906741	MCF10A-Er-Src	breast:	n/a
30	chr4:2906691-2906741	ovcar-3	ovarian:	n/a
31	chr4:2906769-2906819	T-47D	breast:	n/a
32	chr4:2906870-2906920	SAEC	small airway:	n/a
33	chr4:2906870-2906920	NHDF-neo	bronchial:	n/a
34	chr4:2906691-2906741	BE2_C	brain:	n/a
35	chr4:2906769-2906819	NHBE	bronchial:	n/a
36	chr4:2906870-2906920	PrEC	prostate:	n/a
37	chr4:2906870-2906920	ProgFib	skin:	n/a
38	chr4:2906769-2906819	HEK293	kidney:	embryo
39	chr4:2906769-2906819	CMK	blood:	n/a
40	chr4:2906769-2906819	NT2-D1	testis:	n/a
41	chr4:2906691-2906741	HMEC	breast:	n/a
42	chr4:2906769-2906819	AG10803	skin:	n/a
43	chr4:2906870-2906920	HCF	heart:	n/a
44	chr4:2906769-2906819	HCT-116	colon:	n/a
45	chr4:2906769-2906819	HRE	kidney:	n/a
46	chr4:2906769-2906819	AoSMC	blood vessel:	n/a
47	chr4:2906691-2906741	PFSK-1	brain:	n/a
48	chr4:2906691-2906741	SKMC	muscle:	n/a
49	chr4:2906870-2906920	AoSMC	blood vessel:	n/a
50	chr4:2906769-2906819	LNCaP	prostate:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2909857..2911472-chr4:2925477..2927647,2	K562	blood:
2	chr4:2906552..2911481-chr4:2934891..2942965,11	MCF-7	breast:
3	chr4:2905536..2909706-chr4:2929255..2933631,5	MCF-7	breast:
4	chr4:2907975..2910281-chr4:2941881..2943677,2	MCF-7	breast:
5	chr4:2747700..2749457-chr4:2908529..2910128,2	MCF-7	breast:
6	chr4:2897346..2900302-chr4:2903352..2905568,2	MCF-7	breast:
7	chr4:2905184..2907605-chr4:2907928..2912349,4	MCF-7	breast:
8	chr4:2756761..2759408-chr4:2907595..2910762,3	MCF-7	breast:
9	chr4:2910030..2912082-chr4:2925815..2928784,2	MCF-7	breast:
10	chr4:2901261..2903208-chr4:2909740..2911464,2	MCF-7	breast:
11	chr4:2905184..2907605-chr4:2907928..2912349,4	MCF-7	breast:
12	chr4:2887075..2889687-chr4:2908396..2910139,2	MCF-7	breast:
13	chr4:2795938..2798748-chr4:2909831..2911364,2	MCF-7	breast:
14	chr4:2910312..2912100-chr4:2912243..2913801,2	MCF-7	breast:
15	chr4:2892098..2895386-chr4:2900898..2904479,3	K562	blood:
16	chr4:2846050..2847976-chr4:2912063..2913866,2	MCF-7	breast:
17	chr4:2908128..2910686-chr4:2915793..2918014,2	MCF-7	breast:
18	chr4:2913655..2916522-chr4:2935033..2937103,2	MCF-7	breast:
19	chr4:2898305..2901238-chr4:2907549..2909946,2	K562	blood:
20	chr4:2883697..2886623-chr4:2900900..2904831,4	MCF-7	breast:
21	chr4:2910312..2912100-chr4:2912243..2913801,2	MCF-7	breast:
22	chr4:2903718..2915473-chr4:2930612..2941584,27	MCF-7	breast:

No data

Variant related genes	Relation type
ADD1	TF binding region
ADD1	CpG island
ENSG00000087274	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000087269	chromatin interactions
ENSG00000249673	chromatin interactions

Extended variants
information (count: 443 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559312342	chr4:2904167-2904168	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs560626235	chr4:2904188-2904189	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs57174035	chr4:2904192-2904193	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs540212260	chr4:2904193-2904194	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs7664801	chr4:2904203-2904204	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532389747	chr4:2904204-2904205	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs181639464	chr4:2904240-2904241	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs186435987	chr4:2904247-2904248	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs150906802	chr4:2904268-2904269	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559468181	chr4:2904285-2904286	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs561956217	chr4:2904292-2904293	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs191525676	chr4:2904352-2904353	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs547726342	chr4:2904381-2904382	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs530263393	chr4:2904486-2904487	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs111412027	chr4:2904531-2904532	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs182468693	chr4:2904542-2904543	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs186785214	chr4:2904554-2904555	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs541950828	chr4:2904556-2904557	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs189692212	chr4:2904581-2904582	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs138985443	chr4:2904588-2904589	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs183242508	chr4:2904609-2904610	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574430004	chr4:2904621-2904622	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs368904672	chr4:2904624-2904625	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs187562626	chr4:2904707-2904708	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs370712525	chr4:2904709-2904710	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs563404152	chr4:2904729-2904730	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs540303479	chr4:2904753-2904754	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs199843059	chr4:2904764-2904765	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553700474	chr4:2904765-2904766	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs577078329	chr4:2904771-2904772	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs546151800	chr4:2904786-2904787	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs531406219	chr4:2904795-2904796	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192933726	chr4:2904817-2904818	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562770198	chr4:2904823-2904824	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs149877200	chr4:2904962-2904963	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs11737419	chr4:2905002-2905003	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs185167577	chr4:2905030-2905031	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs562044512	chr4:2905042-2905043	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs527761160	chr4:2905123-2905124	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs375089191	chr4:2905131-2905132	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs188291989	chr4:2905149-2905150	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs80214675	chr4:2905160-2905161	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs533136123	chr4:2905292-2905293	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs147572748	chr4:2905344-2905345	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs570002737	chr4:2905357-2905358	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs140385389	chr4:2905392-2905393	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549538316	chr4:2905400-2905401	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs144336184	chr4:2905407-2905408	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs568085173	chr4:2905437-2905438	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs192980658	chr4:2905460-2905461	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Breast cancer	21785460	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2870200-2914000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:2876600-2919200	Strong transcription	Primary B cells from peripheral blood	blood
3	chr4:2877200-2919400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:2880600-2915000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:2883600-2918600	Strong transcription	Fetal Stomach	stomach
6	chr4:2890400-2918000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:2893000-2907800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr4:2893000-2919400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:2893200-2907600	Strong transcription	Primary T cells from cord blood	blood
10	chr4:2893200-2907600	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr4:2893200-2914000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr4:2893200-2918800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr4:2893200-2918800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr4:2893200-2919200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr4:2893200-2932600	Strong transcription	Fetal Thymus	thymus
16	chr4:2893400-2915800	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr4:2893400-2918800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:2893400-2919000	Strong transcription	Fetal Muscle Leg	muscle
19	chr4:2893800-2909200	Strong transcription	Lung	lung
20	chr4:2893800-2918600	Strong transcription	Thymus	Thymus
21	chr4:2893800-2919000	Strong transcription	Duodenum Mucosa	Duodenum
22	chr4:2894000-2923000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:2894400-2907600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr4:2894600-2907600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr4:2894800-2919800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:2895000-2907600	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr4:2895000-2917800	Strong transcription	Dnd41	blood
28	chr4:2895200-2907800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr4:2895200-2915000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:2895200-2919000	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr4:2895400-2907800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr4:2895400-2908200	Strong transcription	HepG2	liver
33	chr4:2895400-2913000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:2895400-2915200	Strong transcription	Placenta	Placenta
35	chr4:2895400-2916200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:2895400-2919000	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:2895600-2905400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:2895600-2914000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr4:2895600-2914200	Strong transcription	GM12878-XiMat	blood
40	chr4:2895600-2915000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:2895600-2918400	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr4:2895600-2919200	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr4:2895600-2919200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:2895800-2909000	Strong transcription	Liver	Liver
45	chr4:2895800-2919000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:2895800-2919200	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr4:2895800-2919200	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr4:2896400-2911800	Strong transcription	Left Ventricle	heart
49	chr4:2896400-2917000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:2896400-2918000	Strong transcription	HSMMtube	muscle

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