Variant report

Variant	nsv997690
Chromosome Location	chr4:102397296-102758125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1719)
CpG islands
(count:733)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1719 , 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	chr4:102695953-102696345	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:102610369-102610662	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:102651772-102651979	HepG2	liver:	n/a	n/a
4	ATF2	chr4:102448264-102448795	GM12878	blood:	n/a	n/a
5	ATF2	chr4:102711518-102712077	GM12878	blood:	n/a	n/a
6	ATF2	chr4:102711410-102712088	GM12878	blood:	n/a	n/a
7	ATF2	chr4:102727996-102728516	GM12878	blood:	n/a	n/a
8	ATF2	chr4:102448337-102448789	GM12878	blood:	n/a	n/a
9	ATF2	chr4:102727971-102728551	GM12878	blood:	n/a	n/a
10	BACH1	chr4:102549349-102549363	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:102703727-102703964	GM12878	blood:	n/a	chr4:102703836-102703847
12	BATF	chr4:102728011-102728377	GM12878	blood:	n/a	chr4:102728254-102728263
13	BATF	chr4:102448356-102448673	GM12878	blood:	n/a	n/a
14	BATF	chr4:102711635-102711995	GM12878	blood:	n/a	n/a
15	BATF	chr4:102713420-102713648	GM12878	blood:	n/a	chr4:102713504-102713512
16	BATF	chr4:102713427-102713837	GM12878	blood:	n/a	chr4:102713504-102713512
17	BATF	chr4:102448397-102448668	GM12878	blood:	n/a	n/a
18	BATF	chr4:102728054-102728394	GM12878	blood:	n/a	chr4:102728254-102728263
19	BATF	chr4:102651652-102651967	GM12878	blood:	n/a	n/a
20	BATF	chr4:102614944-102615380	GM12878	blood:	n/a	chr4:102615272-102615282
21	BCL11A	chr4:102448389-102448769	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:102711557-102711983	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
23	BCL11A	chr4:102728103-102728355	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:102448409-102448610	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:102711669-102711979	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
26	BCL11A	chr4:102728040-102728390	GM12878	blood:	n/a	n/a
27	BCL3	chr4:102728039-102728486	GM12878	blood:	n/a	n/a
28	BCL3	chr4:102711691-102711970	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
29	BCL3	chr4:102711661-102712049	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
30	BCLAF1	chr4:102711548-102712021	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
31	BCLAF1	chr4:102448357-102448663	GM12878	blood:	n/a	n/a
32	BCLAF1	chr4:102711441-102712085	GM12878	blood:	n/a	chr4:102711814-102711823 chr4:102711945-102711954
33	BHLHE40	chr4:102711628-102712010	GM12878	blood:	n/a	chr4:102711991-102712007
34	BHLHE40	chr4:102448368-102448702	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:102645420-102645722	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:102728061-102728467	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:102728731-102728861	GM12878	blood:	n/a	n/a
38	BRCA1	chr4:102518518-102518591	GM12878	blood:	n/a	n/a
39	BRCA1	chr4:102756835-102756998	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr4:102564519-102564546	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr4:102513235-102513369	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr4:102678590-102678637	GM12878	blood:	n/a	n/a
43	CBX3	chr4:102692873-102693335	HCT-116	colon:	n/a	n/a
44	CBX3	chr4:102651391-102652158	HCT-116	colon:	n/a	n/a
45	CBX3	chr4:102627818-102628253	HCT-116	colon:	n/a	n/a
46	CEBPB	chr4:102716847-102717325	A549	lung:	n/a	chr4:102717046-102717057 chr4:102717066-102717077
47	CEBPB	chr4:102674951-102675224	H1-hESC	embryonic stem cell:	n/a	chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090 chr4:102675081-102675090
48	CEBPB	chr4:102756667-102757029	IMR90	lung:	n/a	chr4:102756836-102756849
49	CEBPB	chr4:102520770-102521106	A549	lung:	n/a	n/a
50	CEBPB	chr4:102448349-102448794	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102734752-102734802	HUVEC	blood vessel:	n/a
2	chr4:102734752-102734802	HUVEC	blood vessel:	n/a
3	chr4:102745414-102745464	A549	lung:	n/a
4	chr4:102712010-102712060	GM06990	blood:	n/a
5	chr4:102715139-102715189	AG09319	gingival:	n/a
6	chr4:102709336-102709386	A549	lung:	n/a
7	chr4:102737794-102737844	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:102737794-102737844	ovcar-3	ovarian:	n/a
9	chr4:102745414-102745464	HEK293	kidney:	embryo
10	chr4:102711773-102711823	SK-N-SH	brain:	n/a
11	chr4:102712397-102712447	HEEpiC	esophagus:	n/a
12	chr4:102712216-102712266	ProgFib	skin:	n/a
13	chr4:102737794-102737844	CMK	blood:	n/a
14	chr4:102711702-102711752	SK-N-MC	brain:	n/a
15	chr4:102734752-102734802	AG09309	skin:	n/a
16	chr4:102734752-102734802	HRPEpiC	eye:	n/a
17	chr4:102712082-102712132	HIPEpiC	eye:	n/a
18	chr4:102712397-102712447	AoSMC	blood vessel:	n/a
19	chr4:102737794-102737844	IMR90	lung:	fetal
20	chr4:102734752-102734802	A549	lung:	n/a
21	chr4:102734752-102734802	IMR90	lung:	fetal
22	chr4:102715139-102715189	HCPEpiC	choroid plexus:	n/a
23	chr4:102712216-102712266	GM12892	blood:	n/a
24	chr4:102712010-102712060	IMR90	lung:	fetal
25	chr4:102734752-102734802	HCPEpiC	choroid plexus:	n/a
26	chr4:102712010-102712060	HCM	heart:	n/a
27	chr4:102734752-102734802	BJ	skin:	n/a
28	chr4:102709336-102709386	BE2_C	brain:	n/a
29	chr4:102712216-102712266	HRE	kidney:	n/a
30	chr4:102745414-102745464	T-47D	breast:	n/a
31	chr4:102712216-102712266	U87	brain:	n/a
32	chr4:102745414-102745464	Caco-2	colon:	n/a
33	chr4:102711773-102711823	ProgFib	skin:	n/a
34	chr4:102709336-102709386	MCF-7	breast:	n/a
35	chr4:102712216-102712266	NHBE	bronchial:	n/a
36	chr4:102712216-102712266	PANC-1	pancreas:	n/a
37	chr4:102715139-102715189	HCM	heart:	n/a
38	chr4:102715139-102715189	SAEC	small airway:	n/a
39	chr4:102715139-102715189	HCT-116	colon:	n/a
40	chr4:102745414-102745464	HCF	heart:	n/a
41	chr4:102712216-102712266	HIPEpiC	eye:	n/a
42	chr4:102711773-102711823	HRCEpiC	kidney:	n/a
43	chr4:102715139-102715189	H1-hESC	embryonic stem cell:	embryo
44	chr4:102712010-102712060	SK-N-SH	brain:	n/a
45	chr4:102711747-102711797	PFSK-1	brain:	n/a
46	chr4:102709336-102709386	SAEC	small airway:	n/a
47	chr4:102712397-102712447	AG09319	gingival:	n/a
48	chr4:102745414-102745464	NB4	blood:	n/a
49	chr4:102745414-102745464	HEEpiC	esophagus:	n/a
50	chr4:102711702-102711752	ovcar-3	ovarian:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:102473957..102475564-chr4:102477066..102478830,2	MCF-7	breast:
2	chr4:102090452..102090967-chr4:102651453..102652195,2	MCF-7	breast:
3	chr4:102228684..102230512-chr4:102715753..102717632,2	K562	blood:
4	chr4:102090081..102090815-chr4:102518241..102518832,2	MCF-7	breast:
5	chr4:102575240..102577315-chr4:102579878..102582255,2	K562	blood:
6	chr4:102151616..102153523-chr4:102648348..102650655,2	MCF-7	breast:
7	chr4:102679449..102682204-chr4:102682535..102685384,2	K562	blood:
8	chr4:102739568..102742034-chr4:102748015..102750811,2	K562	blood:
9	chr4:102340377..102343341-chr4:102516987..102519019,2	MCF-7	breast:
10	chr4:102432296..102434415-chr4:102447007..102448829,2	MCF-7	breast:
11	chr4:102537582..102540434-chr4:102541822..102544690,2	K562	blood:
12	chr4:102267789..102270313-chr4:102518098..102520924,2	MCF-7	breast:
13	chr4:102575240..102577315-chr4:102579878..102582255,2	K562	blood:
14	chr4:102668209..102669910-chr4:102674187..102676043,2	MCF-7	breast:
15	chr4:102540601..102543394-chr4:102544865..102546483,2	MCF-7	breast:
16	chr4:102465283..102467753-chr4:102468417..102470025,2	MCF-7	breast:
17	chr4:102748202..102750922-chr4:102785267..102786848,2	MCF-7	breast:
18	chr4:102679449..102682204-chr4:102682535..102685384,2	K562	blood:
19	chr4:102432296..102434415-chr4:102447007..102448829,2	MCF-7	breast:
20	chr4:102755518..102758333-chr4:102759339..102760873,2	MCF-7	breast:
21	chr4:102266409..102268590-chr4:102516202..102517720,2	MCF-7	breast:
22	chr4:102465283..102467753-chr4:102468417..102470025,2	MCF-7	breast:
23	chr4:102705460..102706994-chr4:102708122..102710097,2	MCF-7	breast:
24	chr4:102537582..102540434-chr4:102541822..102544690,2	K562	blood:
25	chr4:102271777..102274738-chr4:102516515..102519508,3	MCF-7	breast:
26	chr4:102090091..102091062-chr4:102651393..102652212,3	MCF-7	breast:
27	chr4:102756033..102758603-chr4:102759128..102761662,3	MCF-7	breast:
28	chr4:102439215..102441659-chr4:102442690..102444241,2	MCF-7	breast:
29	chr4:102439215..102441659-chr4:102442690..102444241,2	MCF-7	breast:
30	chr4:102705460..102706994-chr4:102708122..102710097,2	MCF-7	breast:
31	chr4:102540601..102543394-chr4:102544865..102546483,2	MCF-7	breast:
32	chr4:102668209..102669910-chr4:102674187..102676043,2	MCF-7	breast:
33	chr4:102519275..102521968-chr4:102570862..102572539,2	K562	blood:
34	chr1:116314786..116315654-chr4:102694925..102695632,2	MCF-7	breast:
35	chr4:102519275..102521968-chr4:102570862..102572539,2	K562	blood:
36	chr4:102473957..102475564-chr4:102477066..102478830,2	MCF-7	breast:
37	chr4:102739568..102742034-chr4:102748015..102750811,2	K562	blood:

No data

Variant related genes	Relation type
BANK1	TF binding region
RNU6-462P	TF binding region
BANK1	CpG island
RNU6-462P	CpG island
ENSG00000153064	chromatin interactions
ENSG00000138814	chromatin interactions
ENSG00000254531	chromatin interactions

Extended variants
information (count: 8051 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:8051 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75024101	chr4:102397810-102397811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558205739	chr4:102397883-102397884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564069807	chr4:102397886-102397887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6840572	chr4:102397930-102397931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553254659	chr4:102397997-102397998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115227775	chr4:102398003-102398004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536131517	chr4:102398022-102398023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574596675	chr4:102398026-102398027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569245602	chr4:102398065-102398066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542015254	chr4:102398091-102398092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569762207	chr4:102398092-102398093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376218936	chr4:102398096-102398097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375798319	chr4:102398134-102398135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111628643	chr4:102398150-102398151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371800156	chr4:102398151-102398152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192857943	chr4:102398165-102398166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371186086	chr4:102398167-102398168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6841188	chr4:102398183-102398184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565369286	chr4:102398198-102398199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6841673	chr4:102398208-102398209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs147477648	chr4:102398215-102398216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572821416	chr4:102398217-102398218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140014535	chr4:102398224-102398225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530299273	chr4:102398260-102398261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6823484	chr4:102398304-102398305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs536832372	chr4:102398312-102398313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34898783	chr4:102398362-102398363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566749429	chr4:102398363-102398364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116737129	chr4:102398398-102398399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6846469	chr4:102398446-102398447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570449113	chr4:102398479-102398480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537850031	chr4:102398498-102398499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374065579	chr4:102398614-102398615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555845087	chr4:102398636-102398637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574692360	chr4:102398642-102398643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535718914	chr4:102398676-102398677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554093249	chr4:102398819-102398820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11940448	chr4:102398828-102398829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72682932	chr4:102398864-102398865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546019648	chr4:102398917-102398918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116045149	chr4:102398929-102398930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544091858	chr4:102398999-102399000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577228853	chr4:102399057-102399058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144257490	chr4:102399060-102399061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6847894	chr4:102399093-102399094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530086364	chr4:102399109-102399110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370857295	chr4:102399122-102399123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548503627	chr4:102399135-102399136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560400604	chr4:102399151-102399152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148717611	chr4:102399170-102399171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
myeloid cancer	21057493	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102397800-102422000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:102406800-102407200	Enhancers	Fetal Thymus	thymus
3	chr4:102421800-102422200	Enhancers	NHEK	skin
4	chr4:102422000-102422400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:102422000-102423000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:102422000-102423200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:102435600-102437600	Enhancers	Fetal Heart	heart
8	chr4:102447600-102449000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr4:102447600-102449000	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr4:102447600-102449200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr4:102447800-102449200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:102447800-102449200	Enhancers	Primary T cells from cord blood	blood
13	chr4:102447800-102449200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr4:102448000-102448200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
15	chr4:102448000-102448600	Enhancers	Primary T cells fromperipheralblood	blood
16	chr4:102448000-102449000	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr4:102448000-102449000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr4:102448000-102449000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr4:102448000-102449200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr4:102448200-102448800	Enhancers	Dnd41	blood
21	chr4:102448200-102449000	Enhancers	GM12878-XiMat	blood
22	chr4:102448200-102449200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr4:102448200-102449200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr4:102448400-102448800	Enhancers	Primary B cells from peripheral blood	blood
25	chr4:102449000-102449200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr4:102453400-102455400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:102455000-102455400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:102455400-102456400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:102456800-102457800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:102460800-102462200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:102479000-102479400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:102480800-102481200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:102481000-102485200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:102485200-102485400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:102485400-102487400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:102487400-102488000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:102491800-102492400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:102492000-102492400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:102492000-102492400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:102492000-102492400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:102492000-102492400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:102497200-102497600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:102497200-102497600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:102501600-102515000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:102505200-102505600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr4:102513600-102514000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:102514800-102515200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr4:102515000-102515600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:102515200-102517800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:102515600-102520600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links