Variant report

Variant	esv3515702
Chromosome Location	chr4:749002-754800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:611)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr4:754456-754736	K562	blood:	n/a	n/a
2	CTCF	chr4:754580-754730	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr4:753720-753870	HBMEC	blood vessel:	n/a	n/a
4	E2F6	chr4:753711-753871	K562	blood:	n/a	n/a
5	E2F6	chr4:753649-754094	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr4:753669-754012	H1-hESC	embryonic stem cell:	n/a	n/a
7	HMGN3	chr4:754479-754630	K562	blood:	n/a	n/a
8	HMGN3	chr4:751002-751175	K562	blood:	n/a	n/a
9	JUND	chr4:752692-752851	HepG2	liver:	n/a	n/a
10	JUND	chr4:753635-753883	H1-hESC	embryonic stem cell:	n/a	n/a
11	JUND	chr4:753010-753169	HepG2	liver:	n/a	n/a
12	JUND	chr4:752012-752612	H1-hESC	embryonic stem cell:	n/a	n/a
13	JUND	chr4:753525-753646	HepG2	liver:	n/a	n/a
14	JUND	chr4:753667-753858	H1-hESC	embryonic stem cell:	n/a	n/a
15	JUND	chr4:752012-752518	H1-hESC	embryonic stem cell:	n/a	n/a
16	JUND	chr4:753441-753551	H1-hESC	embryonic stem cell:	n/a	n/a
17	PBX3	chr4:749160-749300	GM12878	blood:	n/a	n/a
18	POLR2A	chr4:751369-751503	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr4:753753-754077	K562	blood:	n/a	n/a
20	POLR2A	chr4:754404-754761	K562	blood:	n/a	n/a
21	POLR2A	chr4:751998-752042	MCF-7	breast:	n/a	n/a
22	POLR2A	chr4:750966-751057	A549	lung:	n/a	n/a
23	POLR2A	chr4:753739-764687	K562	blood:	n/a	n/a
24	POLR2A	chr4:753868-753893	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr4:751425-751478	MCF-7	breast:	n/a	n/a
26	POLR2A	chr4:751057-751269	K562	blood:	n/a	n/a
27	POLR2A	chr4:750673-751396	MCF-7	breast:	n/a	n/a
28	POLR2A	chr4:750823-751164	U87	brain:	n/a	n/a
29	POLR2A	chr4:750697-751204	GM12878	blood:	n/a	n/a
30	POLR2A	chr4:753760-754183	MCF-7	breast:	n/a	n/a
31	POLR2A	chr4:749762-750209	HepG2	liver:	n/a	n/a
32	POLR2A	chr4:748316-749286	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:753019-754283	K562	blood:	n/a	n/a
34	POLR2A	chr4:750745-751215	U87	brain:	n/a	n/a
35	POLR2A	chr4:753734-759040	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:754578-755005	GM12878	blood:	n/a	n/a
37	POLR2A	chr4:748168-749236	HepG2	liver:	n/a	n/a
38	POLR2A	chr4:754463-755193	SK-N-MC	brain:	n/a	n/a
39	POLR2A	chr4:750976-751156	GM12878	blood:	n/a	n/a
40	POLR2A	chr4:747752-749330	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr4:753789-754734	GM12878	blood:	n/a	n/a
42	POLR2A	chr4:750482-750730	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr4:752140-752159	MCF-7	breast:	n/a	n/a
44	POLR2A	chr4:751098-751100	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr4:750423-750607	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr4:750846-750997	K562	blood:	n/a	n/a
47	POLR2A	chr4:751108-751159	HepG2	liver:	n/a	n/a
48	POLR2A	chr4:750916-751258	U87	brain:	n/a	n/a
49	POLR2A	chr4:754238-754341	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr4:752060-752124	MCF-7	breast:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:753903-753953	H1-hESC	embryonic stem cell:	embryo
2	chr4:753903-753953	H1-hESC	embryonic stem cell:	embryo
3	chr4:754410-754460	LNCaP	prostate:	n/a
4	chr4:749139-749189	T-47D	breast:	n/a
5	chr4:749157-749207	GM19239	blood:	n/a
6	chr4:749157-749207	HNPCEpiC	eye:	n/a
7	chr4:751071-751121	HNPCEpiC	eye:	n/a
8	chr4:754733-754783	ECC-1	luminal epithelium:	n/a
9	chr4:749139-749189	ECC-1	luminal epithelium:	n/a
10	chr4:754410-754460	Jurkat	blood:	n/a
11	chr4:749139-749189	HMEC	breast:	n/a
12	chr4:749157-749207	NB4	blood:	n/a
13	chr4:751205-751255	MCF-7	breast:	n/a
14	chr4:753903-753953	AG10803	skin:	n/a
15	chr4:749248-749298	HAEpiC	amniotic membrane:	n/a
16	chr4:749139-749189	HRCEpiC	kidney:	n/a
17	chr4:751048-751098	Caco-2	colon:	n/a
18	chr4:749139-749189	A549	lung:	n/a
19	chr4:753903-753953	HEK293	kidney:	embryo
20	chr4:751071-751121	AG04449	skin:	fetal
21	chr4:753903-753953	IMR90	lung:	fetal
22	chr4:751048-751098	HUVEC	blood vessel:	n/a
23	chr4:750851-750901	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:751205-751255	Jurkat	blood:	n/a
25	chr4:750851-750901	BJ	skin:	n/a
26	chr4:751048-751098	LNCaP	prostate:	n/a
27	chr4:749248-749298	NH-A	brain:	n/a
28	chr4:754733-754783	GM19239	blood:	n/a
29	chr4:751205-751255	HRPEpiC	eye:	n/a
30	chr4:751048-751098	SK-N-SH_RA	brain:	n/a
31	chr4:750851-750901	HUVEC	blood vessel:	n/a
32	chr4:751048-751098	H1-hESC	embryonic stem cell:	embryo
33	chr4:749139-749189	HCF	heart:	n/a
34	chr4:754733-754783	H1-hESC	embryonic stem cell:	embryo
35	chr4:754733-754783	GM12891	blood:	n/a
36	chr4:751071-751121	NHBE	bronchial:	n/a
37	chr4:754410-754460	SK-N-MC	brain:	n/a
38	chr4:749157-749207	ECC-1	luminal epithelium:	n/a
39	chr4:751048-751098	HCPEpiC	choroid plexus:	n/a
40	chr4:749139-749189	HEEpiC	esophagus:	n/a
41	chr4:754410-754460	SK-N-SH_RA	brain:	n/a
42	chr4:754410-754460	HepG2	liver:	n/a
43	chr4:754410-754460	AG10803	skin:	n/a
44	chr4:751071-751121	T-47D	breast:	n/a
45	chr4:751205-751255	H1-hESC	embryonic stem cell:	embryo
46	chr4:751205-751255	SK-N-SH	brain:	n/a
47	chr4:751048-751098	GM06990	blood:	n/a
48	chr4:749139-749189	MCF-7	breast:	n/a
49	chr4:749139-749189	NHDF-neo	bronchial:	n/a
50	chr4:749139-749189	GM12892	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:736307..738718-chr4:749075..751030,2	K562	blood:
2	chr4:747711..750407-chr4:773806..776789,2	MCF-7	breast:
3	chr4:666788..669425-chr4:753705..755956,2	K562	blood:
4	chr4:658116..660628-chr4:754612..756376,2	K562	blood:
5	chr4:741902..744115-chr4:754225..756300,2	MCF-7	breast:
6	chr4:736682..739540-chr4:747411..749398,2	MCF-7	breast:
7	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
8	chr4:593904..597020-chr4:753917..757326,3	MCF-7	breast:
9	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
10	chr4:745543..747300-chr4:747376..749196,2	K562	blood:
11	chr4:754637..757120-chr4:925087..927511,3	MCF-7	breast:
12	chr4:746706..749416-chr4:774128..775692,2	MCF-7	breast:
13	chr4:749591..753567-chr4:753955..757140,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPLX1-8	chr4:750810-751528	ENSG00000272588.1
2	lnc-CPLX1-4	chr4:753969-754335	predAs_ge08_PCGF3_2
3	lnc-CPLX1-8	chr4:751179-751731	expRegAs_chr4_73_-
4	lnc-CPLX1-9	chr4:750116-750354	expRegAs_chr4_71_-

No data

Variant related genes	Relation type
ENSG00000272588	TF binding region
ENSG00000272588	CpG island
ENSG00000133256	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000272588	chromatin interactions
ENSG00000215375	chromatin interactions

Extended variants
information (count: 367 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577107862	chr4:749049-749050	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544556661	chr4:749051-749052	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs75412477	chr4:749058-749059	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs574401458	chr4:749071-749072	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541432204	chr4:749077-749078	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs140748435	chr4:749078-749079	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566605625	chr4:749112-749113	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs150477896	chr4:749116-749117	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145371117	chr4:749123-749124	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs149182543	chr4:749127-749128	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs17722012	chr4:749128-749129	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79911023	chr4:749136-749137	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181413520	chr4:749140-749141	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530126025	chr4:749142-749143	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548250402	chr4:749144-749145	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185995388	chr4:749158-749159	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs549566564	chr4:749161-749162	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534078200	chr4:749193-749194	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35422727	chr4:749233-749234	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs71604318	chr4:749238-749239	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368320229	chr4:749243-749244	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552692871	chr4:749245-749246	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372641471	chr4:749246-749247	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567914411	chr4:749248-749249	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs28549702	chr4:749249-749250	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs189604623	chr4:749256-749257	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs556520097	chr4:749259-749260	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574610676	chr4:749286-749287	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs182255621	chr4:749293-749294	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553441203	chr4:749303-749304	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs187568961	chr4:749306-749307	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571999172	chr4:749308-749309	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545529289	chr4:749316-749317	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs563817393	chr4:749454-749455	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577046002	chr4:749546-749547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368624080	chr4:749561-749562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538563127	chr4:749615-749616	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190908675	chr4:749618-749619	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77937203	chr4:749620-749621	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548862792	chr4:749634-749635	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560323751	chr4:749648-749649	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs55662514	chr4:749701-749702	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201127038	chr4:749710-749711	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570528684	chr4:749712-749713	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75592533	chr4:749720-749721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183672069	chr4:749736-749737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527668367	chr4:749749-749750	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143098102	chr4:749767-749768	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570926690	chr4:749777-749778	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571653659	chr4:749778-749779	Weak transcription Strong transcription	Chromatin interactive region	2 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
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:702200-754800	Weak transcription	Hela-S3	cervix
2	chr4:715600-750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:727000-767600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr4:728600-755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr4:728600-763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:729000-754600	Weak transcription	Fetal Kidney	kidney
7	chr4:729000-762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:729600-753800	Weak transcription	Psoas Muscle	Psoas
9	chr4:729600-760800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:733600-753800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:736600-752000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr4:741400-749200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:741400-749400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:741400-749400	Strong transcription	Thymus	Thymus
15	chr4:741400-749600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr4:741400-749600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr4:741400-751000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:741400-751400	Strong transcription	Fetal Brain Female	brain
19	chr4:741400-751800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:741400-752000	Strong transcription	Fetal Intestine Small	intestine
21	chr4:741400-752400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:741400-752400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:741400-752800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:741400-752800	Strong transcription	Fetal Thymus	thymus
25	chr4:741600-749200	Strong transcription	Primary T cells from cord blood	blood
26	chr4:741600-749400	Strong transcription	Gastric	stomach
27	chr4:741600-749400	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr4:741600-750400	Strong transcription	Fetal Lung	lung
29	chr4:741600-750600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr4:741600-750800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:741600-751200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr4:741600-751600	Strong transcription	Dnd41	blood
33	chr4:741600-752400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr4:741600-752400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:741600-752400	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr4:741600-752800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:741800-749200	Strong transcription	Duodenum Mucosa	Duodenum
38	chr4:741800-751800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr4:742200-749200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:742200-749200	ZNF genes & repeats	Fetal Stomach	stomach
41	chr4:742200-749600	Strong transcription	Stomach Smooth Muscle	stomach
42	chr4:742600-751800	Strong transcription	Placenta	Placenta
43	chr4:742600-754400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:742600-763600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr4:742800-754200	Weak transcription	Colon Smooth Muscle	Colon
46	chr4:742800-756200	Weak transcription	Stomach Mucosa	stomach
47	chr4:742800-764000	Weak transcription	Small Intestine	intestine
48	chr4:743400-749400	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr4:743800-749400	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr4:743800-749400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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