Variant report

Variant	nsv834634
Chromosome Location	chr3:22420053-22574021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:123)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 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	BACH1	chr3:22565441-22565729	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:22565581-22565648	K562	blood:	n/a	n/a
3	BHLHE40	chr3:22526923-22526941	GM12878	blood:	n/a	n/a
4	CEBPB	chr3:22461953-22462276	A549	lung:	n/a	chr3:22462116-22462127
5	CEBPB	chr3:22522316-22522614	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:22533921-22533924	K562	blood:	n/a	n/a
7	CEBPB	chr3:22461971-22462246	HepG2	liver:	n/a	chr3:22462116-22462127
8	CEBPB	chr3:22419951-22420223	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:22522306-22522616	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:22522295-22522589	A549	lung:	n/a	n/a
11	CEBPB	chr3:22559473-22559665	HepG2	liver:	n/a	chr3:22559626-22559637
12	CTCF	chr3:22517420-22517570	HPF	lung:	n/a	n/a
13	CTCF	chr3:22502588-22502712	Lung_OC	lung:	n/a	n/a
14	CTCF	chr3:22481540-22481690	GM12873	blood:	n/a	n/a
15	CTCF	chr3:22560831-22560877	Lung_OC	lung:	n/a	n/a
16	CTCF	chr3:22484317-22484341	GM10266	blood:	n/a	n/a
17	CTCF	chr3:22551200-22551350	K562	blood:	n/a	n/a
18	CTCF	chr3:22481586-22481720	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr3:22423219-22423304	GM20000	blood:	n/a	n/a
20	CTCF	chr3:22481540-22481690	HEK293	kidney:	n/a	n/a
21	CTCF	chr3:22449080-22449114	GM10266	blood:	n/a	n/a
22	CTCF	chr3:22426085-22426120	LNCaP	prostate:	n/a	n/a
23	CTCF	chr3:22503480-22503690	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr3:22475900-22476050	HepG2	liver:	n/a	n/a
25	CTCF	chr3:22535692-22535744	Lung_OC	lung:	n/a	n/a
26	CTCF	chr3:22455440-22455590	HepG2	liver:	n/a	n/a
27	CTCF	chr3:22423241-22423280	GM10266	blood:	n/a	n/a
28	CTCF	chr3:22459244-22459356	LNCaP	prostate:	n/a	n/a
29	CTCF	chr3:22450319-22450368	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:22495780-22495930	NHLF	lung:	n/a	n/a
31	CTCF	chr3:22544560-22544710	GM12801	blood:	n/a	n/a
32	E2F4	chr3:22516092-22516481	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr3:22543291-22543607	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr3:22518923-22519197	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr3:22465905-22466012	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr3:22499539-22499754	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr3:22555303-22555503	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr3:22433470-22433653	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr3:22516988-22517602	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr3:22521863-22522063	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr3:22424046-22424270	GM12878	blood:	n/a	n/a
42	EBF1	chr3:22517237-22517537	GM12878	blood:	n/a	n/a
43	EBF1	chr3:22444843-22444918	GM12878	blood:	n/a	n/a
44	EP300	chr3:22516066-22516830	SK-N-SH	brain:	n/a	chr3:22516154-22516162 chr3:22516104-22516111
45	EP300	chr3:22516171-22516581	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr3:22423723-22423883	GM12878	blood:	n/a	n/a
47	EP300	chr3:22492450-22492890	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr3:22492576-22492911	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr3:22441129-22441339	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr3:22492450-22493015	SK-N-SH	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22423260-22423310	CMK	blood:	n/a
2	chr3:22423260-22423310	CMK	blood:	n/a
3	chr3:22423260-22423310	A549	lung:	n/a
4	chr3:22423260-22423310	HCT-116	colon:	n/a
5	chr3:22423260-22423310	AoSMC	blood vessel:	n/a
6	chr3:22422855-22422905	GM19239	blood:	n/a
7	chr3:22423260-22423310	AG09319	gingival:	n/a
8	chr3:22423260-22423310	HCM	heart:	n/a
9	chr3:22423260-22423310	HCF	heart:	n/a
10	chr3:22422855-22422905	Hela-S3	cervix:	n/a
11	chr3:22422855-22422905	NH-A	brain:	n/a
12	chr3:22422855-22422905	ovcar-3	ovarian:	n/a
13	chr3:22423260-22423310	HUVEC	blood vessel:	n/a
14	chr3:22423260-22423310	HNPCEpiC	eye:	n/a
15	chr3:22423260-22423310	T-47D	breast:	n/a
16	chr3:22422855-22422905	Hepatocyte	liver:	n/a
17	chr3:22422855-22422905	HL-60	blood:	n/a
18	chr3:22423260-22423310	HepG2	liver:	n/a
19	chr3:22422855-22422905	HRE	kidney:	n/a
20	chr3:22423260-22423310	BJ	skin:	n/a
21	chr3:22422855-22422905	PFSK-1	brain:	n/a
22	chr3:22422855-22422905	HCPEpiC	choroid plexus:	n/a
23	chr3:22422855-22422905	AG04450	lung:	fetal
24	chr3:22423260-22423310	GM19239	blood:	n/a
25	chr3:22423260-22423310	NHBE	bronchial:	n/a
26	chr3:22422855-22422905	AG04449	skin:	fetal
27	chr3:22423260-22423310	IMR90	lung:	fetal
28	chr3:22422855-22422905	LNCaP	prostate:	n/a
29	chr3:22422855-22422905	HEEpiC	esophagus:	n/a
30	chr3:22423260-22423310	AG04450	lung:	fetal
31	chr3:22422855-22422905	NHDF-neo	bronchial:	n/a
32	chr3:22422855-22422905	NHBE	bronchial:	n/a
33	chr3:22422855-22422905	HIPEpiC	eye:	n/a
34	chr3:22423260-22423310	H1-hESC	embryonic stem cell:	embryo
35	chr3:22422855-22422905	HAEpiC	amniotic membrane:	n/a
36	chr3:22422855-22422905	HCM	heart:	n/a
37	chr3:22423260-22423310	Hela-S3	cervix:	n/a
38	chr3:22422855-22422905	MCF-7	breast:	n/a
39	chr3:22423260-22423310	HRE	kidney:	n/a
40	chr3:22423260-22423310	PFSK-1	brain:	n/a
41	chr3:22423260-22423310	HEK293	kidney:	embryo
42	chr3:22423260-22423310	GM12891	blood:	n/a
43	chr3:22423260-22423310	GM12878	blood:	n/a
44	chr3:22423260-22423310	SAEC	small airway:	n/a
45	chr3:22423260-22423310	ProgFib	skin:	n/a
46	chr3:22422855-22422905	AG09319	gingival:	n/a
47	chr3:22423260-22423310	K562	blood:	n/a
48	chr3:22422855-22422905	Jurkat	blood:	n/a
49	chr3:22422855-22422905	AG09309	skin:	n/a
50	chr3:22423260-22423310	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:22499125..22501406-chr3:22508186..22509688,2	K562	blood:
2	chr3:22454300..22456299-chr3:22460627..22462261,2	K562	blood:
3	chr3:22501026..22503450-chr3:22509731..22511752,2	K562	blood:
4	chr3:22531342..22533092-chr3:22535706..22538633,2	K562	blood:
5	chr3:22420213..22422752-chr3:22425859..22427632,2	K562	blood:
6	chr3:22454300..22456299-chr3:22460627..22462261,2	K562	blood:
7	chr3:22527480..22530262-chr3:22542907..22545144,2	K562	blood:
8	chr3:22420213..22422752-chr3:22425859..22427632,2	K562	blood:
9	chr3:22531582..22534400-chr3:23151408..23153228,2	K562	blood:
10	chr3:22501026..22503450-chr3:22509731..22511752,2	K562	blood:
11	chr3:22531342..22533092-chr3:22535706..22538633,2	K562	blood:
12	chr3:22499125..22501406-chr3:22508186..22509688,2	K562	blood:
13	chr3:22527480..22530262-chr3:22542907..22545144,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF385D-2	chr3:22495716-22495905	l_2331_chr3:22495715-22498151_testes
2	lnc-ZNF385D-2	chr3:22498045-22498151	l_2331_chr3:22495715-22498151_testes
3	lnc-UBE2E2-6	chr3:22424046-22424420	NONHSAT088657

No data

Variant related genes	Relation type
HMGB1P5	TF binding region
HMGB1P5	CpG island

Extended variants
information (count: 1665 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116437889	chr3:22420063-22420064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184969061	chr3:22420070-22420071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554989500	chr3:22420078-22420079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs79791633	chr3:22420112-22420113	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs543930582	chr3:22420143-22420144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565380056	chr3:22420194-22420195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577327926	chr3:22420213-22420214	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373913402	chr3:22420239-22420240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs147040849	chr3:22421807-22421808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62247342	chr3:22421812-22421813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs533247479	chr3:22421864-22421865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552567953	chr3:22421868-22421869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535479590	chr3:22421897-22421898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535157791	chr3:22421932-22421933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553148482	chr3:22421943-22421944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373195490	chr3:22421949-22421950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12629017	chr3:22421958-22421959	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs114505169	chr3:22421959-22421960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3762777	chr3:22421971-22421972	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs3762778	chr3:22422207-22422208	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs115944622	chr3:22422212-22422213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73144166	chr3:22422229-22422230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs9310692	chr3:22422272-22422273	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35999639	chr3:22422286-22422287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564512340	chr3:22422290-22422291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528426924	chr3:22422302-22422303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546709160	chr3:22422305-22422306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9310693	chr3:22422334-22422335	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs187969493	chr3:22422335-22422336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541015776	chr3:22422337-22422338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199672442	chr3:22422348-22422349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550810652	chr3:22422391-22422392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs3749374	chr3:22422856-22422857	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569440899	chr3:22422894-22422895	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs139762619	chr3:22422954-22422955	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs369972381	chr3:22423018-22423019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs534471367	chr3:22423035-22423036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555447127	chr3:22423038-22423039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs563638050	chr3:22423044-22423045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77815321	chr3:22423051-22423052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs537945665	chr3:22423061-22423062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3749375	chr3:22423131-22423132	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs577789614	chr3:22423132-22423133	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544840947	chr3:22423138-22423139	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs143128570	chr3:22423140-22423141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs146672077	chr3:22423146-22423147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542504312	chr3:22423153-22423154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs183587857	chr3:22423165-22423166	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs571063209	chr3:22423166-22423167	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529203844	chr3:22423177-22423178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22421800-22422000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:22422200-22422400	Enhancers	Fetal Lung	lung
3	chr3:22429800-22430400	Enhancers	Fetal Lung	lung
4	chr3:22432000-22432800	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr3:22440800-22442000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:22457600-22458800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:22458000-22458800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr3:22458200-22458600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:22460600-22461200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:22460600-22461200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:22473000-22473400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:22473000-22473600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:22491400-22492800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr3:22491400-22493400	Enhancers	Thymus	Thymus
15	chr3:22491400-22493800	Enhancers	Dnd41	blood
16	chr3:22491400-22497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:22491800-22493400	Enhancers	Fetal Lung	lung
18	chr3:22491800-22493800	Enhancers	Primary hematopoietic stem cells	blood
19	chr3:22492000-22492600	Enhancers	Fetal Stomach	stomach
20	chr3:22492000-22493400	Enhancers	Fetal Thymus	thymus
21	chr3:22492200-22492400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:22492200-22492600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr3:22492200-22493000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr3:22492200-22493200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:22492200-22493400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:22492400-22492800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:22492600-22493200	Enhancers	Adipose Nuclei	Adipose
28	chr3:22492800-22493200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:22492800-22493400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:22493200-22494800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:22493200-22494800	Weak transcription	Adipose Nuclei	Adipose
32	chr3:22493200-22497200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:22493400-22494800	Weak transcription	Fetal Thymus	thymus
34	chr3:22493400-22495000	Weak transcription	Fetal Lung	lung
35	chr3:22493400-22495000	Weak transcription	Thymus	Thymus
36	chr3:22493800-22495000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr3:22494800-22495200	Enhancers	Fetal Thymus	thymus
38	chr3:22494800-22496000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:22494800-22496000	Enhancers	Adipose Nuclei	Adipose
40	chr3:22495000-22495800	Enhancers	Primary hematopoietic stem cells	blood
41	chr3:22495000-22495800	Enhancers	Thymus	Thymus
42	chr3:22495000-22497000	Enhancers	Fetal Lung	lung
43	chr3:22497200-22498200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:22498200-22498400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr3:22499000-22499200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr3:22499200-22499400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:22510400-22512000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:22510600-22512200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:22511400-22511800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr3:22511800-22517200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links