Variant report

Variant	nsv595145
Chromosome Location	chr4:110969572-110982248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:110971107-110971511	GM12878	blood:	n/a	n/a
2	ATF2	chr4:110976581-110977022	GM12878	blood:	n/a	n/a
3	ATF2	chr4:110980803-110981343	GM12878	blood:	n/a	n/a
4	ATF2	chr4:110976395-110977114	GM12878	blood:	n/a	n/a
5	ATF2	chr4:110980641-110981338	GM12878	blood:	n/a	n/a
6	BACH1	chr4:110976699-110977049	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:110976570-110977021	GM12878	blood:	n/a	chr4:110976578-110976587
8	BATF	chr4:110980834-110981230	GM12878	blood:	n/a	n/a
9	BATF	chr4:110980885-110981260	GM12878	blood:	n/a	n/a
10	BATF	chr4:110977439-110977669	GM12878	blood:	n/a	n/a
11	BATF	chr4:110976658-110976951	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:110980773-110981382	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:110976453-110977103	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:110980633-110981103	GM12878	blood:	n/a	n/a
15	CEBPB	chr4:110977040-110977331	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:110976509-110977148	GM12878	blood:	n/a	n/a
17	CHD1	chr4:110980780-110981030	GM12878	blood:	n/a	n/a
18	CHD1	chr4:110971012-110971639	IMR90	lung:	n/a	n/a
19	CHD2	chr4:110981063-110981217	GM12878	blood:	n/a	n/a
20	CHD2	chr4:110976594-110977052	GM12878	blood:	n/a	n/a
21	CREB1	chr4:110980698-110981563	GM12878	blood:	n/a	n/a
22	CTCF	chr4:110971180-110971330	HEK293	kidney:	n/a	n/a
23	CTCF	chr4:110971067-110971502	GM12878	blood:	n/a	n/a
24	CTCF	chr4:110971119-110971436	A549	lung:	n/a	n/a
25	CTCF	chr4:110971180-110971330	BJ	skin:	n/a	n/a
26	CTCF	chr4:110971200-110971350	A549	lung:	n/a	n/a
27	CTCF	chr4:110971129-110971347	A549	lung:	n/a	n/a
28	CTCF	chr4:110971180-110971330	GM12801	blood:	n/a	n/a
29	CTCF	chr4:110971114-110971431	A549	lung:	n/a	n/a
30	CTCF	chr4:110971147-110971417	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr4:110971200-110971350	HMEC	breast:	n/a	n/a
32	CTCF	chr4:110971180-110971330	GM12867	blood:	n/a	n/a
33	CTCF	chr4:110971128-110971432	Medullo	brain:	n/a	n/a
34	CTCF	chr4:110971220-110971370	GM12878	blood:	n/a	n/a
35	CTCF	chr4:110971196-110971369	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr4:110971200-110971350	NHEK	skin:	n/a	n/a
37	CTCF	chr4:110971166-110971415	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:110971180-110971330	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:110971142-110971410	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr4:110971180-110971330	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr4:110971135-110971579	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:110971160-110971411	HepG2	liver:	n/a	n/a
43	CTCF	chr4:110971103-110971407	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr4:110971160-110971430	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:110971220-110971370	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr4:110971236-110971331	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:110971220-110971370	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr4:110971200-110971350	HAc	cerebellar:	n/a	n/a
49	CTCF	chr4:110971180-110971330	GM12866	blood:	n/a	n/a
50	CTCF	chr4:110971144-110971416	HUVEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110971665-110971715	GM12891	blood:	n/a
2	chr4:110971665-110971715	SK-N-SH	brain:	n/a
3	chr4:110971665-110971715	A549	lung:	n/a
4	chr4:110971665-110971715	HCM	heart:	n/a
5	chr4:110971665-110971715	HAEpiC	amniotic membrane:	n/a
6	chr4:110971665-110971715	Caco-2	colon:	n/a
7	chr4:110971665-110971715	GM06990	blood:	n/a
8	chr4:110971665-110971715	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:110971665-110971715	SAEC	small airway:	n/a
10	chr4:110971665-110971715	U87	brain:	n/a
11	chr4:110971665-110971715	HEEpiC	esophagus:	n/a
12	chr4:110971665-110971715	BJ	skin:	n/a
13	chr4:110971665-110971715	NB4	blood:	n/a
14	chr4:110971665-110971715	Jurkat	blood:	n/a
15	chr4:110971665-110971715	MCF-7	breast:	n/a
16	chr4:110971665-110971715	GM19239	blood:	n/a
17	chr4:110971665-110971715	NHBE	bronchial:	n/a
18	chr4:110971665-110971715	AG04450	lung:	fetal
19	chr4:110971665-110971715	HIPEpiC	eye:	n/a
20	chr4:110971665-110971715	HEK293	kidney:	embryo
21	chr4:110971665-110971715	NHDF-neo	bronchial:	n/a
22	chr4:110971665-110971715	T-47D	breast:	n/a
23	chr4:110971665-110971715	NT2-D1	testis:	n/a
24	chr4:110971665-110971715	GM12892	blood:	n/a
25	chr4:110971665-110971715	HCF	heart:	n/a
26	chr4:110971665-110971715	HRE	kidney:	n/a
27	chr4:110971665-110971715	HL-60	blood:	n/a
28	chr4:110971665-110971715	RPTEC	kidney:	n/a
29	chr4:110971665-110971715	GM12878	blood:	n/a
30	chr4:110971665-110971715	SKMC	muscle:	n/a
31	chr4:110971665-110971715	AG10803	skin:	n/a
32	chr4:110971665-110971715	IMR90	lung:	fetal
33	chr4:110971665-110971715	HepG2	liver:	n/a
34	chr4:110971665-110971715	HNPCEpiC	eye:	n/a
35	chr4:110971665-110971715	LNCaP	prostate:	n/a
36	chr4:110971665-110971715	AG09309	skin:	n/a
37	chr4:110971665-110971715	PrEC	prostate:	n/a
38	chr4:110971665-110971715	HCT-116	colon:	n/a
39	chr4:110971665-110971715	K562	blood:	n/a
40	chr4:110971665-110971715	HUVEC	blood vessel:	n/a
41	chr4:110971665-110971715	HCPEpiC	choroid plexus:	n/a
42	chr4:110971665-110971715	AoSMC	blood vessel:	n/a
43	chr4:110971665-110971715	BE2_C	brain:	n/a
44	chr4:110971665-110971715	SK-N-MC	brain:	n/a
45	chr4:110971665-110971715	NH-A	brain:	n/a
46	chr4:110971665-110971715	HRCEpiC	kidney:	n/a
47	chr4:110971665-110971715	HRPEpiC	eye:	n/a
48	chr4:110971665-110971715	CMK	blood:	n/a
49	chr4:110971665-110971715	Hela-S3	cervix:	n/a
50	chr4:110971665-110971715	AG04449	skin:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:110972268..110974968-chr4:110975889..110979455,3	K562	blood:
2	chr4:110982174..110983963-chr4:111117469..111119843,2	K562	blood:
3	chr4:110970781..110971308-chr4:111132291..111133109,2	K562	blood:
4	chr4:110966949..110970337-chr4:111117054..111120581,3	MCF-7	breast:
5	chr4:110975742..110978325-chr4:111114327..111116572,2	K562	blood:
6	chr4:110970810..110971311-chr4:111431767..111432274,2	K562	blood:
7	chr4:110975222..110976850-chr4:111118540..111120184,2	MCF-7	breast:
8	chr4:110970906..110974111-chr4:111117676..111120910,5	MCF-7	breast:
9	chr4:110970036..110972230-chr4:111118255..111121131,3	MCF-7	breast:
10	chr4:110972268..110974968-chr4:110975889..110979455,3	K562	blood:
11	chr4:110978929..110981764-chr4:111118255..111120738,2	K562	blood:
12	chr4:110977785..110984731-chr4:111116105..111121044,7	MCF-7	breast:
13	chr4:110972756..110975536-chr4:111115190..111118473,3	MCF-7	breast:
14	chr4:110971182..110971957-chr4:111132272..111132881,2	MCF-7	breast:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ELOVL6	hsa-miR-211-5p	chr4:110970701-110970695
2	ELOVL6	hsa-miR-92a-3p	chr4:110971269-110971291
3	ELOVL6	hsa-miR-204-5p	chr4:110970701-110970695
4	ELOVL6	hsa-miR-211-5p	chr4:110971101-110971122
5	ELOVL6	hsa-miR-92a-3p	chr4:110970246-110970268
6	ELOVL6	hsa-miR-204-5p	chr4:110971101-110971122
7	ELOVL6	hsa-miR-204-5p	chr4:110970695-110970714
8	ELOVL6	hsa-miR-92a-3p	chr4:110970252-110970245
9	ELOVL6	hsa-miR-211-5p	chr4:110970695-110970716

Variant related genes	Relation type
ELOVL6	TF binding region
ELOVL6	CpG island
ENSG00000170522	chromatin interactions

Extended variants
information (count: 465 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11947713	chr4:110969572-110969573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6837303	chr4:110969585-110969586	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549889965	chr4:110969678-110969679	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569568522	chr4:110969692-110969693	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76994049	chr4:110969705-110969706	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548605725	chr4:110969721-110969722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568698025	chr4:110969754-110969755	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534212587	chr4:110969798-110969799	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371403454	chr4:110969799-110969800	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs200600528	chr4:110969862-110969863	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201125372	chr4:110969872-110969873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553973813	chr4:110969873-110969874	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182982006	chr4:110969929-110969930	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559147140	chr4:110969931-110969932	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577253726	chr4:110969965-110969966	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539559804	chr4:110969999-110970000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556209861	chr4:110970026-110970027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34313935	chr4:110970035-110970036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576360429	chr4:110970036-110970037	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542164464	chr4:110970046-110970047	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17041272	chr4:110970082-110970083	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572349635	chr4:110970148-110970149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553056114	chr4:110970156-110970157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564310937	chr4:110970162-110970163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61539771	chr4:110970240-110970241	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574892029	chr4:110970253-110970254	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
27	rs543566561	chr4:110970255-110970256	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
28	rs139201207	chr4:110970267-110970268	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
29	rs367677624	chr4:110970312-110970313	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188054700	chr4:110970320-110970321	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549003968	chr4:110970352-110970353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371671518	chr4:110970414-110970415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565536616	chr4:110970474-110970475	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373446008	chr4:110970503-110970504	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs547651252	chr4:110970511-110970512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570732322	chr4:110970513-110970514	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539597504	chr4:110970620-110970621	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144020419	chr4:110970635-110970636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570170830	chr4:110970644-110970645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558476235	chr4:110970688-110970689	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200193952	chr4:110970699-110970700	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
42	rs150566425	chr4:110970706-110970707	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
43	rs542097308	chr4:110970739-110970740	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572458055	chr4:110970763-110970764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs193007746	chr4:110970765-110970766	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs578103697	chr4:110970772-110970773	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539871927	chr4:110970810-110970811	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143429080	chr4:110970811-110970812	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375119711	chr4:110970838-110970839	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs28450072	chr4:110970851-110970852	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110963400-110972600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr4:110963400-110976200	Weak transcription	Fetal Intestine Large	intestine
3	chr4:110963600-110971000	Weak transcription	Liver	Liver
4	chr4:110963800-110974600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr4:110964600-110971200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:110964600-110971200	Weak transcription	Brain Angular Gyrus	brain
7	chr4:110964600-110971200	Weak transcription	HepG2	liver
8	chr4:110964600-110971400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:110964600-110972000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:110964600-110972000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:110964600-110972000	Weak transcription	HSMM	muscle
12	chr4:110964600-110972200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr4:110964600-110975200	Weak transcription	Fetal Heart	heart
14	chr4:110964600-110976600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:110964600-110976600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:110964600-110981000	Weak transcription	Adipose Nuclei	Adipose
17	chr4:110964600-110981800	Weak transcription	Brain Anterior Caudate	brain
18	chr4:110964600-111004000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:110964800-110969600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr4:110964800-110970200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:110964800-110971400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:110964800-110976400	Weak transcription	Fetal Kidney	kidney
23	chr4:110964800-110982800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr4:110965000-110972200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:110965000-110974200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:110965000-110982000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:110965200-110976600	Weak transcription	HSMMtube	muscle
28	chr4:110965200-110986600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:110965400-110970800	Weak transcription	K562	blood
30	chr4:110965400-110994200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:110965600-110971600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr4:110966000-110971400	Weak transcription	NHLF	lung
33	chr4:110966000-110972600	Weak transcription	NHEK	skin
34	chr4:110966200-110970800	Weak transcription	Dnd41	blood
35	chr4:110966600-110972200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:110966600-110972400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr4:110966800-110974000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:110966800-110982000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:110967600-110980000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:110967800-110971400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr4:110967800-110976600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:110968000-110971400	Weak transcription	Fetal Stomach	stomach
43	chr4:110968000-110972000	Weak transcription	NH-A	brain
44	chr4:110968000-110976600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:110968200-110969600	Weak transcription	Brain Germinal Matrix	brain
46	chr4:110968200-110970200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr4:110968200-110970200	Weak transcription	Brain Hippocampus Middle	brain
48	chr4:110968200-110971200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:110968200-110972000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr4:110968200-110972200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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