Variant report

Variant	nsv999411
Chromosome Location	chr4:25701-59060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1705)
CpG islands
(count:795)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1705 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:28478-28706	K562	blood:	n/a	n/a
2	ARID3A	chr4:29032-29969	K562	blood:	n/a	n/a
3	ARID3A	chr4:27798-27995	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:40826-41573	K562	blood:	n/a	n/a
5	ARID3A	chr4:55074-62562	K562	blood:	n/a	chr4:59934-59950 chr4:59538-59554
6	ARID3A	chr4:50859-54863	K562	blood:	n/a	n/a
7	ARID3A	chr4:36835-37141	K562	blood:	n/a	n/a
8	ATF1	chr4:44475-45429	K562	blood:	n/a	n/a
9	ATF1	chr4:47552-48360	K562	blood:	n/a	n/a
10	ATF1	chr4:49243-50168	K562	blood:	n/a	n/a
11	ATF1	chr4:42873-44116	K562	blood:	n/a	n/a
12	ATF1	chr4:53699-58079	K562	blood:	n/a	n/a
13	ATF1	chr4:58355-59701	K562	blood:	n/a	n/a
14	ATF1	chr4:50536-53493	K562	blood:	n/a	n/a
15	ATF1	chr4:40925-41405	K562	blood:	n/a	n/a
16	ATF1	chr4:36415-36470	K562	blood:	n/a	n/a
17	ATF1	chr4:35776-36199	K562	blood:	n/a	n/a
18	ATF1	chr4:36709-37394	K562	blood:	n/a	n/a
19	ATF1	chr4:46422-47217	K562	blood:	n/a	n/a
20	ATF1	chr4:28608-30088	K562	blood:	n/a	n/a
21	ATF2	chr4:51468-52077	GM12878	blood:	n/a	n/a
22	ATF3	chr4:51522-52289	K562	blood:	n/a	n/a
23	BACH1	chr4:35874-36136	K562	blood:	n/a	n/a
24	BACH1	chr4:46413-47194	K562	blood:	n/a	n/a
25	BACH1	chr4:52750-53412	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:27939-28273	K562	blood:	n/a	n/a
27	BACH1	chr4:55097-61002	K562	blood:	n/a	n/a
28	BACH1	chr4:47659-50155	K562	blood:	n/a	n/a
29	BACH1	chr4:28837-29898	K562	blood:	n/a	n/a
30	BACH1	chr4:36609-36633	K562	blood:	n/a	n/a
31	BACH1	chr4:36885-37510	K562	blood:	n/a	n/a
32	BACH1	chr4:40109-40248	K562	blood:	n/a	n/a
33	BACH1	chr4:50515-54873	K562	blood:	n/a	n/a
34	BATF	chr4:26654-26993	GM12878	blood:	n/a	n/a
35	BATF	chr4:28657-28916	GM12878	blood:	n/a	n/a
36	BATF	chr4:26720-26981	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:51522-52034	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:28657-28950	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:26950-27116	GM12878	blood:	n/a	chr4:27018-27026
40	BCL3	chr4:57268-58100	K562	blood:	n/a	n/a
41	BCL3	chr4:51572-51881	GM12878	blood:	n/a	n/a
42	BCL3	chr4:58347-59453	K562	blood:	n/a	n/a
43	BCLAF1	chr4:54975-57752	K562	blood:	n/a	n/a
44	BDP1	chr4:55568-56251	Hela-S3	cervix:	n/a	n/a
45	BDP1	chr4:47688-48887	Hela-S3	cervix:	n/a	n/a
46	BDP1	chr4:50490-52141	Hela-S3	cervix:	n/a	n/a
47	BDP1	chr4:42890-44145	Hela-S3	cervix:	n/a	n/a
48	BDP1	chr4:54340-59681	K562	blood:	n/a	chr4:55208-55217
49	BDP1	chr4:46325-47270	Hela-S3	cervix:	n/a	n/a
50	BDP1	chr4:57211-58198	Hela-S3	cervix:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:53115-53165	AoSMC	blood vessel:	n/a
2	chr4:50006-50056	HCF	heart:	n/a
3	chr4:53115-53165	AoSMC	blood vessel:	n/a
4	chr4:50006-50056	HCF	heart:	n/a
5	chr4:53115-53165	Hepatocyte	liver:	n/a
6	chr4:53548-53598	HepG2	liver:	n/a
7	chr4:53264-53314	MCF-7	breast:	n/a
8	chr4:53146-53196	PFSK-1	brain:	n/a
9	chr4:53264-53314	HEEpiC	esophagus:	n/a
10	chr4:53025-53075	HCPEpiC	choroid plexus:	n/a
11	chr4:53548-53598	A549	lung:	n/a
12	chr4:53025-53075	SKMC	muscle:	n/a
13	chr4:53010-53060	SAEC	small airway:	n/a
14	chr4:53233-53283	NH-A	brain:	n/a
15	chr4:53270-53320	Caco-2	colon:	n/a
16	chr4:53010-53060	H1-hESC	embryonic stem cell:	embryo
17	chr4:53270-53320	NH-A	brain:	n/a
18	chr4:54036-54086	HNPCEpiC	eye:	n/a
19	chr4:53025-53075	RPTEC	kidney:	n/a
20	chr4:55967-56017	GM06990	blood:	n/a
21	chr4:54036-54086	SK-N-MC	brain:	n/a
22	chr4:53146-53196	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:55967-56017	AG09309	skin:	n/a
24	chr4:50006-50056	SKMC	muscle:	n/a
25	chr4:53233-53283	PANC-1	pancreas:	n/a
26	chr4:53548-53598	MCF10A-Er-Src	breast:	n/a
27	chr4:53264-53314	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:53010-53060	GM06990	blood:	n/a
29	chr4:50006-50056	MCF10A-Er-Src	breast:	n/a
30	chr4:50006-50056	Hela-S3	cervix:	n/a
31	chr4:53010-53060	HRPEpiC	eye:	n/a
32	chr4:53270-53320	U87	brain:	n/a
33	chr4:53115-53165	MCF-7	breast:	n/a
34	chr4:53233-53283	AoSMC	blood vessel:	n/a
35	chr4:55967-56017	HEK293	kidney:	embryo
36	chr4:53264-53314	HMEC	breast:	n/a
37	chr4:53025-53075	HEEpiC	esophagus:	n/a
38	chr4:53025-53075	GM12878	blood:	n/a
39	chr4:53109-53159	AG04449	skin:	fetal
40	chr4:53264-53314	HCPEpiC	choroid plexus:	n/a
41	chr4:53548-53598	PrEC	prostate:	n/a
42	chr4:53115-53165	CMK	blood:	n/a
43	chr4:53010-53060	NHDF-neo	bronchial:	n/a
44	chr4:53010-53060	ovcar-3	ovarian:	n/a
45	chr4:53115-53165	IMR90	lung:	fetal
46	chr4:53548-53598	K562	blood:	n/a
47	chr4:53146-53196	NH-A	brain:	n/a
48	chr4:53233-53283	SKMC	muscle:	n/a
49	chr4:53025-53075	HRCEpiC	kidney:	n/a
50	chr4:54036-54086	Caco-2	colon:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:52592..54684-chr4:123109..125181,3	MCF-7	breast:
2	chr4:26589..30670-chr4:53416..55763,3	K562	blood:
3	chr4:46489..48476-chr4:152002..154876,2	K562	blood:
4	chr4:35105..37664-chr4:54869..57777,2	K562	blood:
5	chr4:35278..37660-chr4:45954..48345,2	K562	blood:
6	chr4:56714..58749-chr8:129715262..129716946,2	MCF-7	breast:
7	chr4:41249..43391-chr4:46700..48279,2	K562	blood:
8	chr20:30618790..30619537-chr4:28922..29754,2	MCF-7	breast:
9	chr4:29168..29759-chr6:156896..157405,3	MCF-7	breast:
10	chr4:27510..29241-chr4:49071..51866,2	K562	blood:
11	chr4:40027..42645-chr4:43576..46121,2	MCF-7	breast:
12	chr4:47548..51523-chr4:51547..55504,6	MCF-7	breast:
13	chr4:28899..29522-chr6:156896..157400,2	MCF-7	breast:
14	chr4:49240..50788-chr4:51565..54254,2	MCF-7	breast:
15	chr4:40027..42645-chr4:43576..46121,2	MCF-7	breast:
16	chr4:56572..58810-chr4:85301..87608,2	K562	blood:
17	chr4:51861..55604-chr4:123095..126398,4	K562	blood:
18	chr4:49240..50788-chr4:51565..54254,2	MCF-7	breast:
19	chr4:26589..30670-chr4:53416..55763,3	K562	blood:
20	chr4:35105..37664-chr4:54869..57777,2	K562	blood:
21	chr4:54876..56789-chr4:65058..66668,2	MCF-7	breast:
22	chr4:35278..37660-chr4:45954..48345,2	K562	blood:
23	chr4:54381..56089-chr4:130547..133394,2	MCF-7	breast:
24	chr4:51557..54446-chr4:122221..124926,2	K562	blood:
25	chr4:27510..30529-chr4:49071..53296,4	K562	blood:
26	chr4:53379..54171-chr4:206857..207651,2	K562	blood:
27	chr4:58315..60128-chr6:30582159..30584362,2	K562	blood:
28	chr4:43139..45301-chr4:52954..54679,2	MCF-7	breast:
29	chr4:41249..43391-chr4:46700..48279,2	K562	blood:
30	chr4:54683..57001-chr4:109535..111840,2	K562	blood:
31	chr4:53253..54771-chr4:331507..334328,2	MCF-7	breast:
32	chr13:115098696..115100218-chr4:35677..37893,2	K562	blood:
33	chr22:29136936..29138528-chr4:45551..48161,2	MCF-7	breast:
34	chr4:28180..30442-chr4:236557..238318,2	MCF-7	breast:
35	chr4:42552..45424-chr4:49559..51220,2	MCF-7	breast:
36	chr4:47548..51523-chr4:51547..55504,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF732-9	chr4:49448-50018	NONHSAT094500
2	lnc-ZNF732-9	chr4:48991-49850	NONHSAT094498
3	lnc-ZNF732-9	chr4:50562-50619	NONHSAT094499
4	lnc-ZNF732-9	chr4:49163-49618	NONHSAT094499

No data

Variant related genes	Relation type
ZNF595	TF binding region
ENSG00000248302	TF binding region
ZNF595	CpG island
ENSG00000248302	CpG island
ENSG00000256143	chromatin interactions
ENSG00000229723	chromatin interactions
ENSG00000248564	chromatin interactions
ENSG00000255436	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000250312	chromatin interactions
ENSG00000248302	chromatin interactions
ENSG00000226239	chromatin interactions
ENSG00000197701	chromatin interactions
ENSG00000131127	chromatin interactions
ENSG00000183765	chromatin interactions

Extended variants
information (count: 1024 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200329525	chr4:25709-25710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548193541	chr4:25741-25742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201579035	chr4:25749-25750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201819458	chr4:25797-25798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200256193	chr4:25805-25806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566806443	chr4:25823-25824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10155269	chr4:25881-25882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527585807	chr4:26131-26132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555981982	chr4:26150-26151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552385461	chr4:26170-26171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376314237	chr4:26178-26179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2213687	chr4:26179-26180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372072993	chr4:26195-26196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2213688	chr4:26202-26203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2213689	chr4:26220-26221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570639684	chr4:26264-26265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2078130	chr4:26490-26491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539158046	chr4:26506-26507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557458871	chr4:26523-26524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569284646	chr4:26551-26552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536695755	chr4:26559-26560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1984426	chr4:26586-26587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554655303	chr4:26600-26601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1988270	chr4:26844-26845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573514401	chr4:26862-26863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540547665	chr4:26970-26971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374617827	chr4:26993-26994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3856983	chr4:27035-27036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2780418	chr4:27134-27135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112368412	chr4:27158-27159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113481057	chr4:27292-27293	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76770332	chr4:27296-27297	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75414024	chr4:27333-27334	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10452298	chr4:27371-27372	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10452284	chr4:27384-27385	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111243424	chr4:27443-27444	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558746060	chr4:27451-27452	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576986468	chr4:27471-27472	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs55966434	chr4:27528-27529	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113321029	chr4:27530-27531	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543910663	chr4:27538-27539	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs202216287	chr4:27539-27540	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs57270711	chr4:27543-27544	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143864777	chr4:27544-27545	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367883839	chr4:27545-27546	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs75808459	chr4:27546-27547	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs10452299	chr4:27548-27549	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562195121	chr4:27550-27551	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs71164490	chr4:27551-27552	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs79349000	chr4:27559-27560	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
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
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18800-27600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:21000-27200	Weak transcription	Dnd41	blood
3	chr4:27200-27400	Enhancers	Adipose Nuclei	Adipose
4	chr4:27200-28000	Enhancers	Dnd41	blood
5	chr4:27200-28800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:27200-29200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:27200-30200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr4:27400-27600	Bivalent Enhancer	Adipose Nuclei	Adipose
9	chr4:27400-29600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:27400-29600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr4:27400-29600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
12	chr4:27400-30000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:27600-27800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
14	chr4:27600-27800	Enhancers	Gastric	stomach
15	chr4:27600-28200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:27600-28200	ZNF genes & repeats	Aorta	Aorta
17	chr4:27600-28200	Bivalent Enhancer	Lung	lung
18	chr4:27600-28200	ZNF genes & repeats	Pancreas	Pancrea
19	chr4:27600-29200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:27600-29400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:27600-29600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:27600-30000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:27600-30200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:27800-28000	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr4:27800-28000	ZNF genes & repeats	Gastric	stomach
26	chr4:27800-28200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:27800-29400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
28	chr4:28000-28200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr4:28000-28200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
30	chr4:28000-28200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
31	chr4:28000-28200	Flanking Active TSS	Dnd41	blood
32	chr4:28000-30000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:28200-28800	Enhancers	Dnd41	blood
34	chr4:28200-29600	Bivalent Enhancer	Adipose Nuclei	Adipose
35	chr4:28400-28800	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr4:28400-29000	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr4:28400-29800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
38	chr4:28400-30000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr4:28400-30000	ZNF genes & repeats	Fetal Brain Male	brain
40	chr4:28600-30000	Enhancers	Primary B cells from peripheral blood	blood
41	chr4:28800-29000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
42	chr4:28800-29000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
43	chr4:28800-29000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr4:28800-29000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr4:28800-29000	Bivalent Enhancer	Left Ventricle	heart
46	chr4:28800-29000	Flanking Bivalent TSS/Enh	Sigmoid Colon	Sigmoid Colon
47	chr4:28800-29200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
48	chr4:28800-29400	ZNF genes & repeats	Thymus	Thymus
49	chr4:28800-29600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr4:28800-29600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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