Variant report

Variant	nsv1003183
Chromosome Location	chr3:19671647-19948351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1342)
CpG islands
(count:612)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:19908154-19908565	K562	blood:	n/a	n/a
2	ARID3A	chr3:19940290-19940486	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:19853257-19853541	K562	blood:	n/a	n/a
4	ARID3A	chr3:19838885-19838997	K562	blood:	n/a	n/a
5	ARID3A	chr3:19930083-19930989	K562	blood:	n/a	n/a
6	ARID3A	chr3:19926931-19927205	K562	blood:	n/a	n/a
7	ARID3A	chr3:19942947-19943100	K562	blood:	n/a	n/a
8	ATF1	chr3:19930581-19931040	K562	blood:	n/a	n/a
9	ATF1	chr3:19785640-19785860	K562	blood:	n/a	n/a
10	ATF2	chr3:19686507-19687102	GM12878	blood:	n/a	n/a
11	ATF2	chr3:19686532-19687019	GM12878	blood:	n/a	n/a
12	ATF3	chr3:19930414-19931207	A549	lung:	n/a	n/a
13	ATF3	chr3:19930543-19931223	A549	lung:	n/a	n/a
14	ATF3	chr3:19908260-19908576	K562	blood:	n/a	n/a
15	BACH1	chr3:19752946-19753205	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:19686696-19686986	H1-hESC	embryonic stem cell:	n/a	chr3:19686699-19686713
17	BACH1	chr3:19853360-19853374	K562	blood:	n/a	n/a
18	BATF	chr3:19811248-19811473	GM12878	blood:	n/a	n/a
19	BATF	chr3:19811274-19811475	GM12878	blood:	n/a	n/a
20	BATF	chr3:19686760-19686968	GM12878	blood:	n/a	chr3:19686837-19686848
21	BATF	chr3:19754546-19754789	GM12878	blood:	n/a	chr3:19754677-19754688
22	BATF	chr3:19686580-19687040	GM12878	blood:	n/a	chr3:19686837-19686848
23	BCL11A	chr3:19811218-19811466	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:19686637-19687019	GM12878	blood:	n/a	n/a
25	BCL3	chr3:19930521-19931308	A549	lung:	n/a	n/a
26	BCL3	chr3:19930434-19931194	A549	lung:	n/a	n/a
27	BHLHE40	chr3:19853210-19853554	K562	blood:	n/a	n/a
28	BHLHE40	chr3:19908238-19908613	K562	blood:	n/a	n/a
29	BHLHE40	chr3:19947424-19947437	K562	blood:	n/a	n/a
30	BHLHE40	chr3:19926880-19927440	K562	blood:	n/a	n/a
31	BHLHE40	chr3:19930409-19931158	K562	blood:	n/a	n/a
32	CBX3	chr3:19853175-19853607	K562	blood:	n/a	n/a
33	CBX3	chr3:19863842-19864085	K562	blood:	n/a	n/a
34	CBX3	chr3:19863896-19864107	K562	blood:	n/a	n/a
35	CBX3	chr3:19930451-19930972	K562	blood:	n/a	n/a
36	CBX3	chr3:19697781-19698060	K562	blood:	n/a	n/a
37	CBX3	chr3:19697778-19698074	K562	blood:	n/a	n/a
38	CCNT2	chr3:19744247-19744413	K562	blood:	n/a	n/a
39	CCNT2	chr3:19853301-19853822	K562	blood:	n/a	n/a
40	CCNT2	chr3:19930425-19931125	K562	blood:	n/a	n/a
41	CCNT2	chr3:19745165-19745410	K562	blood:	n/a	n/a
42	CEBPB	chr3:19773120-19773412	IMR90	lung:	n/a	chr3:19773267-19773278 chr3:19773265-19773278 chr3:19773267-19773276
43	CEBPB	chr3:19715374-19715574	HepG2	liver:	n/a	chr3:19715473-19715484
44	CEBPB	chr3:19771031-19771375	HepG2	liver:	n/a	chr3:19771204-19771215 chr3:19771204-19771217
45	CEBPB	chr3:19761319-19761505	K562	blood:	n/a	chr3:19761369-19761378 chr3:19761369-19761378 chr3:19761367-19761380 chr3:19761369-19761378 chr3:19761367-19761380 chr3:19761369-19761378 chr3:19761367-19761378
46	CEBPB	chr3:19862926-19863121	K562	blood:	n/a	chr3:19862986-19862997
47	CEBPB	chr3:19675337-19675639	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:19862879-19863181	A549	lung:	n/a	chr3:19862986-19862997
49	CEBPB	chr3:19921115-19921434	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:19926899-19927238	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19752610-19752660	AG10803	skin:	n/a
2	chr3:19673982-19674032	HCT-116	colon:	n/a
3	chr3:19752610-19752660	AG10803	skin:	n/a
4	chr3:19673982-19674032	HCT-116	colon:	n/a
5	chr3:19791356-19791406	GM19239	blood:	n/a
6	chr3:19850542-19850592	SK-N-SH	brain:	n/a
7	chr3:19744061-19744111	GM12891	blood:	n/a
8	chr3:19744061-19744111	HAEpiC	amniotic membrane:	n/a
9	chr3:19740602-19740652	AG10803	skin:	n/a
10	chr3:19752610-19752660	AG04449	skin:	fetal
11	chr3:19850542-19850592	NB4	blood:	n/a
12	chr3:19791356-19791406	Caco-2	colon:	n/a
13	chr3:19740602-19740652	MCF10A-Er-Src	breast:	n/a
14	chr3:19791456-19791506	ProgFib	skin:	n/a
15	chr3:19744061-19744111	GM19239	blood:	n/a
16	chr3:19791456-19791506	SK-N-MC	brain:	n/a
17	chr3:19740602-19740652	GM12892	blood:	n/a
18	chr3:19930780-19930830	BE2_C	brain:	n/a
19	chr3:19673982-19674032	U87	brain:	n/a
20	chr3:19791456-19791506	LNCaP	prostate:	n/a
21	chr3:19791304-19791354	SK-N-SH_RA	brain:	n/a
22	chr3:19752610-19752660	HUVEC	blood vessel:	n/a
23	chr3:19673982-19674032	Hela-S3	cervix:	n/a
24	chr3:19930780-19930830	HCM	heart:	n/a
25	chr3:19791304-19791354	HCM	heart:	n/a
26	chr3:19930780-19930830	AG10803	skin:	n/a
27	chr3:19791304-19791354	NHBE	bronchial:	n/a
28	chr3:19791356-19791406	NT2-D1	testis:	n/a
29	chr3:19930780-19930830	CMK	blood:	n/a
30	chr3:19740602-19740652	HIPEpiC	eye:	n/a
31	chr3:19740602-19740652	PFSK-1	brain:	n/a
32	chr3:19850542-19850592	HEK293	kidney:	embryo
33	chr3:19930780-19930830	U87	brain:	n/a
34	chr3:19673982-19674032	ovcar-3	ovarian:	n/a
35	chr3:19791304-19791354	GM12891	blood:	n/a
36	chr3:19673982-19674032	SKMC	muscle:	n/a
37	chr3:19752610-19752660	HepG2	liver:	n/a
38	chr3:19744061-19744111	AG04450	lung:	fetal
39	chr3:19752610-19752660	PrEC	prostate:	n/a
40	chr3:19930780-19930830	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:19752610-19752660	GM19239	blood:	n/a
42	chr3:19740602-19740652	SKMC	muscle:	n/a
43	chr3:19791356-19791406	SAEC	small airway:	n/a
44	chr3:19673982-19674032	CMK	blood:	n/a
45	chr3:19930780-19930830	AG04449	skin:	fetal
46	chr3:19818187-19818237	Caco-2	colon:	n/a
47	chr3:19930780-19930830	SAEC	small airway:	n/a
48	chr3:19930780-19930830	HEEpiC	esophagus:	n/a
49	chr3:19744061-19744111	GM12892	blood:	n/a
50	chr3:19791356-19791406	HL-60	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:
2	chr3:19923874..19927811-chr3:19988482..19992158,4	K562	blood:
3	chr3:19389760..19391334-chr3:19907874..19909391,17	MCF-7	breast:
4	chr3:19936510..19939152-chr3:19987860..19990168,2	MCF-7	breast:
5	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
6	chr3:19087867..19088435-chr3:19907906..19908471,2	MCF-7	breast:
7	chr3:19908798..19910478-chr3:19922117..19924794,2	K562	blood:
8	chr3:19926681..19927540-chr3:20080667..20081886,4	MCF-7	breast:
9	chr3:17936078..17936595-chr3:19908226..19908883,2	K562	blood:
10	chr3:19930617..19933383-chr3:19987388..19990668,4	MCF-7	breast:
11	chr3:19908798..19910478-chr3:19922117..19924794,2	K562	blood:
12	chr3:19926588..19927515-chr3:19942549..19943117,5	MCF-7	breast:
13	chr3:19935726..19938656-chr3:19941159..19945067,3	K562	blood:
14	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
15	chr3:19926646..19927515-chr3:20080662..20081812,4	K562	blood:
16	chr3:19936727..19938285-chr3:19942132..19944334,2	K562	blood:
17	chr3:19930446..19931966-chr3:19932163..19933731,2	MCF-7	breast:
18	chr3:19866393..19868702-chr3:19871331..19874203,2	K562	blood:
19	chr3:19389338..19390161-chr3:19907650..19908872,3	MCF-7	breast:
20	chr3:19801295..19803442-chr3:19807030..19809544,2	K562	blood:
21	chr3:19926588..19927515-chr3:19942549..19943117,5	MCF-7	breast:
22	chr3:19866393..19868702-chr3:19871331..19874203,2	K562	blood:
23	chr3:19106302..19107287-chr3:19907999..19908895,3	MCF-7	breast:
24	chr1:200367178..200368137-chr3:19907997..19908546,2	MCF-7	breast:
25	chr3:19928340..19930933-chr3:19988714..19991654,2	K562	blood:
26	chr3:19747542..19750159-chr3:19752091..19755330,3	MCF-7	breast:
27	chr3:19936727..19938285-chr3:19942132..19944334,2	K562	blood:
28	chr3:19925587..19927827-chr3:19934570..19937110,2	MCF-7	breast:
29	chr3:19926567..19927530-chr3:21592329..21593167,2	MCF-7	breast:
30	chr3:19747542..19750159-chr3:19752091..19755330,3	MCF-7	breast:
31	chr3:19930434..19932349-chr3:19933276..19934867,2	K562	blood:
32	chr3:19930446..19931966-chr3:19932163..19933731,2	MCF-7	breast:
33	chr3:19925587..19927827-chr3:19934570..19937110,2	MCF-7	breast:
34	chr3:19390433..19391079-chr3:19907967..19908843,4	MCF-7	breast:
35	chr3:19926188..19928582-chr3:19987242..19988957,2	MCF-7	breast:
36	chr3:19946568..19948512-chr3:19950144..19952107,2	K562	blood:
37	chr3:19919756..19921311-chr3:20094992..20097825,2	K562	blood:
38	chr3:19935726..19938656-chr3:19941159..19945067,3	K562	blood:
39	chr3:19829915..19832031-chr3:19834488..19836078,2	K562	blood:
40	chr3:19863239..19864953-chr3:20226349..20229139,2	K562	blood:
41	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:
42	chr3:19829915..19832031-chr3:19834488..19836078,2	K562	blood:
43	chr3:19801295..19803442-chr3:19807030..19809544,2	K562	blood:
44	chr3:19922897..19926980-chr3:19987408..19989481,3	MCF-7	breast:
45	chr3:19930434..19932349-chr3:19933276..19934867,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFHB-1	chr3:19729726-19729972	XLOC_003064
2	lnc-EFHB-1	chr3:19717560-19717598	XLOC_003064

No data

Variant related genes	Relation type
EFHB	TF binding region
EFHB	CpG island
ENSG00000129810	chromatin interactions
ENSG00000163576	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000144566	chromatin interactions
ESYT1	miRNA target sites

Extended variants
information (count: 4119 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4119 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142445178	chr3:19672408-19672409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554406352	chr3:19672425-19672426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189847003	chr3:19672470-19672471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543278206	chr3:19672500-19672501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558805885	chr3:19672516-19672517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6787710	chr3:19672573-19672574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541338377	chr3:19672612-19672613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112890017	chr3:19672649-19672650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559684604	chr3:19672675-19672676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530081597	chr3:19672723-19672724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542192824	chr3:19672724-19672725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563659186	chr3:19672766-19672767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531056303	chr3:19672789-19672790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs13071260	chr3:19672807-19672808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs13071268	chr3:19672821-19672822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552218619	chr3:19672849-19672850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570719651	chr3:19672860-19672861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528614180	chr3:19672862-19672863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181109738	chr3:19672863-19672864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9857864	chr3:19672864-19672865	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535901892	chr3:19672877-19672878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115971877	chr3:19672913-19672914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569519756	chr3:19672928-19672929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62278787	chr3:19672936-19672937	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558642404	chr3:19672965-19672966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577157678	chr3:19673082-19673083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145952515	chr3:19673090-19673091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113454462	chr3:19673137-19673138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139799957	chr3:19673189-19673190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574655765	chr3:19673231-19673232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371221488	chr3:19673244-19673245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112496875	chr3:19673293-19673294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115221324	chr3:19673313-19673314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563718187	chr3:19673325-19673326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575508447	chr3:19673378-19673379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545893800	chr3:19673393-19673394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564237825	chr3:19673431-19673432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111379906	chr3:19673482-19673483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528698969	chr3:19673490-19673491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185645723	chr3:19673534-19673535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190451512	chr3:19673550-19673551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550193696	chr3:19673561-19673562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577072461	chr3:19673568-19673569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550954911	chr3:19673617-19673618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569639088	chr3:19673623-19673624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112244748	chr3:19673664-19673665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144543063	chr3:19673677-19673678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545645759	chr3:19673722-19673723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13324034	chr3:19673724-19673725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112956166	chr3:19673752-19673753	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20531469	CNVD

Chromatin state (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19672400-19674400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr3:19673600-19674200	Enhancers	GM12878-XiMat	blood
3	chr3:19673600-19674400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:19673600-19674800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:19674000-19674400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:19674000-19674400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:19674000-19674600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:19674000-19674600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:19674000-19674800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:19674200-19675000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:19683000-19683200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:19683200-19686600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:19685200-19686600	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:19685800-19686600	ZNF genes & repeats	GM12878-XiMat	blood
15	chr3:19686200-19686800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:19686400-19687200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr3:19686600-19686800	Active TSS	GM12878-XiMat	blood
18	chr3:19686800-19687000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:19686800-19687000	Flanking Active TSS	GM12878-XiMat	blood
20	chr3:19687000-19687200	Enhancers	GM12878-XiMat	blood
21	chr3:19693400-19694400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr3:19693600-19694000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr3:19693600-19694000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:19693600-19694200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:19693600-19694400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:19693600-19694600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:19693600-19694600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:19693600-19695000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:19693800-19694800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:19694000-19695000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:19694400-19695000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr3:19694400-19696400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:19694600-19695000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:19696400-19697000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:19697400-19697800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:19712800-19713000	Weak transcription	Spleen	Spleen
37	chr3:19713000-19713400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr3:19724000-19724200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr3:19724200-19743600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr3:19727800-19728200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr3:19730200-19730800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:19740000-19741600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr3:19740200-19740600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:19740200-19740800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:19740200-19741000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:19740200-19741400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr3:19740600-19743600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr3:19741000-19741200	Enhancers	Aorta	Aorta
49	chr3:19741000-19741400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:19741200-19742200	Weak transcription	Aorta	Aorta

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