Variant report

Variant	esv3449469
Chromosome Location	chr7:38283757-38303458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:305)
Chromatin interactive
region (count:1)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
2	ATF1	chr7:38285408-38285488	K562	blood:	n/a	n/a
3	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
4	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
5	ATF1	chr7:38285866-38286066	K562	blood:	n/a	n/a
6	ATF2	chr7:38289493-38289850	GM12878	blood:	n/a	n/a
7	BATF	chr7:38289510-38289833	GM12878	blood:	n/a	n/a
8	BATF	chr7:38289507-38289847	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
10	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
11	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
12	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
13	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
14	CTCF	chr7:38292997-38293033	Lung_OC	lung:	n/a	n/a
15	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
16	CTCF	chr7:38300410-38300476	Fibrobl	skin:	n/a	n/a
17	CTCF	chr7:38288542-38288588	Spleen_OC	spleen:	n/a	n/a
18	E2F4	chr7:38295337-38295499	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr7:38296707-38296986	K562	blood:	n/a	n/a
20	GATA3	chr7:38295488-38295652	SH-SY5Y	brain:	n/a	n/a
21	IRF1	chr7:38295253-38295287	K562	blood:	n/a	n/a
22	IRF4	chr7:38289363-38289945	GM12878	blood:	n/a	n/a
23	IRF4	chr7:38289425-38289865	GM12878	blood:	n/a	n/a
24	JUND	chr7:38296695-38297059	K562	blood:	n/a	n/a
25	JUND	chr7:38301252-38301322	K562	blood:	n/a	n/a
26	MAFK	chr7:38302721-38302861	HepG2	liver:	n/a	n/a
27	MAX	chr7:38298232-38298389	NB4	blood:	n/a	n/a
28	MAX	chr7:38296352-38297047	NB4	blood:	n/a	n/a
29	MYC	chr7:38298360-38298420	NB4	blood:	n/a	n/a
30	MYC	chr7:38296645-38296965	NB4	blood:	n/a	n/a
31	NFYB	chr7:38287843-38288025	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:38297103-38297104	A549	lung:	n/a	n/a
33	POLR2A	chr7:38296900-38297402	HL-60	blood:	n/a	n/a
34	POLR2A	chr7:38298845-38298956	K562	blood:	n/a	n/a
35	POLR2A	chr7:38295611-38297185	HL-60	blood:	n/a	n/a
36	POLR2A	chr7:38287502-38288155	HL-60	blood:	n/a	n/a
37	POLR2A	chr7:38297130-38297137	A549	lung:	n/a	n/a
38	POLR2A	chr7:38284136-38284555	HL-60	blood:	n/a	n/a
39	POLR2A	chr7:38293891-38294206	HL-60	blood:	n/a	n/a
40	POLR2A	chr7:38294274-38294331	Gliobla	brain:	n/a	n/a
41	POLR2A	chr7:38285147-38285616	HL-60	blood:	n/a	n/a
42	POLR2A	chr7:38296137-38296759	HL-60	blood:	n/a	n/a
43	RCOR1	chr7:38285437-38285527	K562	blood:	n/a	n/a
44	RCOR1	chr7:38289585-38289725	GM12878	blood:	n/a	n/a
45	REST	chr7:38289524-38289804	Hela-S3	cervix:	n/a	n/a
46	REST	chr7:38296172-38297062	HL-60	blood:	n/a	n/a
47	SP1	chr7:38289533-38289750	GM12878	blood:	n/a	n/a
48	SPI1	chr7:38289358-38289921	GM12891	blood:	n/a	chr7:38289643-38289656 chr7:38289640-38289649 chr7:38289642-38289655 chr7:38289643-38289656
49	SPI1	chr7:38289355-38289885	GM12891	blood:	n/a	chr7:38289643-38289656 chr7:38289640-38289649 chr7:38289642-38289655 chr7:38289643-38289656
50	SPI1	chr7:38289526-38289739	K562	blood:	n/a	chr7:38289643-38289656 chr7:38289640-38289649 chr7:38289642-38289655 chr7:38289643-38289656

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38298966-38299016	IMR90	lung:	fetal
2	chr7:38296393-38296443	HNPCEpiC	eye:	n/a
3	chr7:38296393-38296443	HAEpiC	amniotic membrane:	n/a
4	chr7:38296393-38296443	GM06990	blood:	n/a
5	chr7:38298966-38299016	AG04449	skin:	fetal
6	chr7:38296393-38296443	NHDF-neo	bronchial:	n/a
7	chr7:38299481-38299531	AG04449	skin:	fetal
8	chr7:38298908-38298958	BE2_C	brain:	n/a
9	chr7:38294113-38294163	HMEC	breast:	n/a
10	chr7:38298908-38298958	ECC-1	luminal epithelium:	n/a
11	chr7:38299481-38299531	NH-A	brain:	n/a
12	chr7:38299481-38299531	K562	blood:	n/a
13	chr7:38294113-38294163	MCF10A-Er-Src	breast:	n/a
14	chr7:38298908-38298958	Jurkat	blood:	n/a
15	chr7:38298908-38298958	H1-hESC	embryonic stem cell:	embryo
16	chr7:38299481-38299531	PFSK-1	brain:	n/a
17	chr7:38294113-38294163	ECC-1	luminal epithelium:	n/a
18	chr7:38299481-38299531	HRPEpiC	eye:	n/a
19	chr7:38294113-38294163	HUVEC	blood vessel:	n/a
20	chr7:38294113-38294163	ProgFib	skin:	n/a
21	chr7:38298908-38298958	HUVEC	blood vessel:	n/a
22	chr7:38294113-38294163	Caco-2	colon:	n/a
23	chr7:38298908-38298958	AG09309	skin:	n/a
24	chr7:38296393-38296443	Jurkat	blood:	n/a
25	chr7:38299481-38299531	SK-N-SH	brain:	n/a
26	chr7:38296393-38296443	HEEpiC	esophagus:	n/a
27	chr7:38294113-38294163	GM19239	blood:	n/a
28	chr7:38298966-38299016	HCM	heart:	n/a
29	chr7:38299481-38299531	HEEpiC	esophagus:	n/a
30	chr7:38298966-38299016	AoSMC	blood vessel:	n/a
31	chr7:38298966-38299016	PANC-1	pancreas:	n/a
32	chr7:38299481-38299531	GM12878	blood:	n/a
33	chr7:38298908-38298958	HCF	heart:	n/a
34	chr7:38299481-38299531	PANC-1	pancreas:	n/a
35	chr7:38294113-38294163	IMR90	lung:	fetal
36	chr7:38294113-38294163	T-47D	breast:	n/a
37	chr7:38296393-38296443	HepG2	liver:	n/a
38	chr7:38298966-38299016	SK-N-SH	brain:	n/a
39	chr7:38298908-38298958	AG10803	skin:	n/a
40	chr7:38294113-38294163	HCPEpiC	choroid plexus:	n/a
41	chr7:38299481-38299531	BJ	skin:	n/a
42	chr7:38298966-38299016	PrEC	prostate:	n/a
43	chr7:38299481-38299531	HNPCEpiC	eye:	n/a
44	chr7:38298908-38298958	GM06990	blood:	n/a
45	chr7:38298966-38299016	GM12878	blood:	n/a
46	chr7:38299481-38299531	HCF	heart:	n/a
47	chr7:38296393-38296443	MCF-7	breast:	n/a
48	chr7:38294113-38294163	BE2_C	brain:	n/a
49	chr7:38296393-38296443	ECC-1	luminal epithelium:	n/a
50	chr7:38296393-38296443	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
2	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
3	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
4	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
5	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
6	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
7	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
8	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
9	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGJP2	TF binding region
TRGJ2	TF binding region
TRGC2	CpG island
TRGJP2	CpG island
TRGJ2	CpG island
ENSG00000211689	chromatin interactions

Extended variants
information (count: 1079 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192429699	chr7:38283765-38283766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373165827	chr7:38283794-38283795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531465998	chr7:38283819-38283820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541833927	chr7:38283826-38283827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386712297	chr7:38283862-38283863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561712944	chr7:38283864-38283865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371600873	chr7:38283873-38283874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527546474	chr7:38283894-38283895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2392541	chr7:38283895-38283896	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs570519526	chr7:38283897-38283898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368348555	chr7:38283902-38283903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372340517	chr7:38283918-38283919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533174430	chr7:38283920-38283921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549593936	chr7:38283930-38283931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4428575	chr7:38283949-38283950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369438471	chr7:38283996-38283997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373253375	chr7:38284000-38284001	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572043852	chr7:38284051-38284052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147232117	chr7:38284057-38284058	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554543595	chr7:38284070-38284071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377267262	chr7:38284088-38284089	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201774131	chr7:38284108-38284109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11973942	chr7:38284113-38284114	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs534187672	chr7:38284114-38284115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201761940	chr7:38284124-38284125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148521992	chr7:38284125-38284126	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554466427	chr7:38284179-38284180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200491725	chr7:38284180-38284181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577493250	chr7:38284181-38284182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4610637	chr7:38284183-38284184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369914552	chr7:38284198-38284199	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs386712298	chr7:38284201-38284202	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144830417	chr7:38284219-38284220	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112160394	chr7:38284240-38284241	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71546636	chr7:38284254-38284255	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs147965655	chr7:38284263-38284264	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565539190	chr7:38284304-38284305	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561483411	chr7:38284306-38284307	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572021631	chr7:38284356-38284357	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76715992	chr7:38284357-38284358	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184761328	chr7:38284363-38284364	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113831189	chr7:38284369-38284370	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564385627	chr7:38284400-38284401	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533091571	chr7:38284405-38284406	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563371464	chr7:38284409-38284410	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549556849	chr7:38284454-38284455	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146656908	chr7:38284472-38284473	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531650295	chr7:38284486-38284487	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548287639	chr7:38284495-38284496	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568330318	chr7:38284498-38284499	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Neuroblastoma	19536264	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38273800-38292200	Weak transcription	Thymus	Thymus
2	chr7:38273800-38305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:38276800-38285800	Weak transcription	Primary T cells from cord blood	blood
4	chr7:38276800-38295600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:38277600-38284200	Weak transcription	Fetal Thymus	thymus
6	chr7:38277600-38292600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr7:38277600-38292600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr7:38278000-38290800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:38278200-38287600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr7:38280800-38284000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr7:38281200-38287200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:38281800-38284000	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr7:38282800-38284200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:38283000-38283800	Weak transcription	Dnd41	blood
15	chr7:38283000-38284400	Weak transcription	K562	blood
16	chr7:38283200-38285400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:38283200-38287800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr7:38283400-38286800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:38283600-38289200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr7:38283800-38289400	Strong transcription	Dnd41	blood
21	chr7:38284000-38284200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr7:38284000-38285600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr7:38284200-38285000	Strong transcription	Fetal Thymus	thymus
24	chr7:38284200-38285800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:38284200-38287000	Genic enhancers	Primary T cells fromperipheralblood	blood
26	chr7:38284400-38284800	Enhancers	K562	blood
27	chr7:38285000-38287600	Weak transcription	Fetal Thymus	thymus
28	chr7:38285400-38286400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr7:38285600-38286800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr7:38285800-38286000	Strong transcription	Primary T cells from cord blood	blood
31	chr7:38285800-38287000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:38286000-38286600	Weak transcription	Primary T cells from cord blood	blood
33	chr7:38286400-38287600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr7:38286600-38288200	Strong transcription	Primary T cells from cord blood	blood
35	chr7:38286800-38287000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr7:38286800-38288200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr7:38287000-38287800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:38287000-38288000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr7:38287000-38288200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
40	chr7:38287200-38288200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr7:38287400-38288000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:38287600-38288000	Strong transcription	Fetal Thymus	thymus
43	chr7:38287600-38288200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:38287600-38288200	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr7:38287800-38288200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr7:38287800-38288200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:38288000-38288200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
48	chr7:38288000-38296200	Weak transcription	Fetal Thymus	thymus
49	chr7:38288200-38289000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr7:38288200-38289200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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