Variant report

Variant	esv3344573
Chromosome Location	chr7:97909166-97912264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97910130-97910572	HepG2	liver:	n/a	n/a
2	ATF3	chr7:97910828-97910981	GM12878	blood:	n/a	chr7:97910851-97910860
3	ATF3	chr7:97910761-97911014	K562	blood:	n/a	chr7:97910803-97910812 chr7:97910851-97910860
4	ATF3	chr7:97910823-97911057	HepG2	liver:	n/a	chr7:97910851-97910860
5	ATF3	chr7:97910805-97911053	GM12878	blood:	n/a	chr7:97910851-97910860
6	ATF3	chr7:97910813-97911050	H1-hESC	embryonic stem cell:	n/a	chr7:97910851-97910860
7	BACH1	chr7:97910074-97910547	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:97910158-97910542	K562	blood:	n/a	chr7:97910241-97910257 chr7:97910487-97910503
9	BHLHE40	chr7:97911312-97911512	GM12878	blood:	n/a	chr7:97911380-97911396
10	BHLHE40	chr7:97911359-97911360	K562	blood:	n/a	n/a
11	BHLHE40	chr7:97910772-97911094	K562	blood:	n/a	chr7:97910794-97910810 chr7:97910791-97910807 chr7:97910825-97910841
12	BHLHE40	chr7:97910134-97911092	GM12878	blood:	n/a	chr7:97910794-97910810 chr7:97910241-97910257 chr7:97910487-97910503 chr7:97910791-97910807 chr7:97910825-97910841
13	BHLHE40	chr7:97910147-97911105	HepG2	liver:	n/a	chr7:97910794-97910810 chr7:97910241-97910257 chr7:97910487-97910503 chr7:97910791-97910807 chr7:97910825-97910841
14	BRCA1	chr7:97910275-97910414	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr7:97910215-97911118	K562	blood:	n/a	chr7:97910598-97910607
16	CEBPB	chr7:97910128-97910155	K562	blood:	n/a	n/a
17	CEBPB	chr7:97909741-97909913	A549	lung:	n/a	chr7:97909864-97909875
18	CEBPB	chr7:97909733-97910227	HepG2	liver:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
19	CEBPB	chr7:97909729-97910198	H1-hESC	embryonic stem cell:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
20	CEBPB	chr7:97909738-97910630	Hela-S3	cervix:	n/a	chr7:97909864-97909875 chr7:97910160-97910173
21	CEBPD	chr7:97910808-97911119	HepG2	liver:	n/a	n/a
22	CEBPD	chr7:97910203-97910784	HepG2	liver:	n/a	n/a
23	CEBPD	chr7:97910342-97910580	HepG2	liver:	n/a	n/a
24	CHD1	chr7:97911400-97911929	GM12878	blood:	n/a	n/a
25	CHD1	chr7:97910882-97912849	IMR90	lung:	n/a	n/a
26	CHD2	chr7:97911727-97911982	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr7:97911395-97911479	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:97910367-97910826	HepG2	liver:	n/a	chr7:97910804-97910814
29	CHD2	chr7:97910151-97910799	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr7:97910393-97910697	GM12878	blood:	n/a	n/a
31	CHD2	chr7:97910284-97911074	Hela-S3	cervix:	n/a	chr7:97910804-97910814
32	CHD2	chr7:97910693-97910733	K562	blood:	n/a	n/a
33	CHD2	chr7:97911462-97911659	GM12878	blood:	n/a	n/a
34	CHD2	chr7:97911874-97912074	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:97911406-97911534	HepG2	liver:	n/a	n/a
36	CREB1	chr7:97910380-97910835	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr7:97911402-97911798	A549	lung:	n/a	n/a
38	CREB1	chr7:97910280-97910719	A549	lung:	n/a	n/a
39	CTCF	chr7:97910276-97910308	Lung_OC	lung:	n/a	chr7:97910294-97910303
40	CTCF	chr7:97910611-97910714	GM12891	blood:	n/a	n/a
41	CTCF	chr7:97910580-97910730	AG04450	lung:	n/a	n/a
42	CTCF	chr7:97910600-97910750	A549	lung:	n/a	n/a
43	CTCF	chr7:97910277-97910314	H1-hESC	embryonic stem cell:	n/a	chr7:97910294-97910303 chr7:97910291-97910309
44	CTCF	chr7:97910180-97910330	HEEpiC	esophagus:	n/a	chr7:97910294-97910303 chr7:97910291-97910309
45	CTCF	chr7:97910360-97910510	HRE	kidney:	n/a	n/a
46	CTCF	chr7:97910560-97910710	HCFaa	heart:	n/a	n/a
47	CTCF	chr7:97910520-97910670	HRE	kidney:	n/a	n/a
48	CTCF	chr7:97910456-97910531	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr7:97910160-97910310	MCF-7	breast:	n/a	chr7:97910294-97910303 chr7:97910291-97910309
50	CTCF	chr7:97910520-97910670	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97910571-97910621	HCF	heart:	n/a
2	chr7:97910571-97910621	HCF	heart:	n/a
3	chr7:97910884-97910934	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:97910884-97910934	GM19239	blood:	n/a
5	chr7:97910808-97910858	CMK	blood:	n/a
6	chr7:97910878-97910928	SK-N-SH	brain:	n/a
7	chr7:97910856-97910906	HIPEpiC	eye:	n/a
8	chr7:97910392-97910442	HL-60	blood:	n/a
9	chr7:97910392-97910442	HMEC	breast:	n/a
10	chr7:97910870-97910920	HCM	heart:	n/a
11	chr7:97910392-97910442	IMR90	lung:	fetal
12	chr7:97910392-97910442	NHDF-neo	bronchial:	n/a
13	chr7:97910808-97910858	IMR90	lung:	fetal
14	chr7:97911512-97911562	Jurkat	blood:	n/a
15	chr7:97912149-97912199	BE2_C	brain:	n/a
16	chr7:97910884-97910934	HMEC	breast:	n/a
17	chr7:97910884-97910934	HRPEpiC	eye:	n/a
18	chr7:97910808-97910858	T-47D	breast:	n/a
19	chr7:97910392-97910442	NT2-D1	testis:	n/a
20	chr7:97911390-97911440	HMEC	breast:	n/a
21	chr7:97910571-97910621	ProgFib	skin:	n/a
22	chr7:97910728-97910778	H1-hESC	embryonic stem cell:	embryo
23	chr7:97911938-97911988	HRCEpiC	kidney:	n/a
24	chr7:97910856-97910906	MCF-7	breast:	n/a
25	chr7:97910808-97910858	HUVEC	blood vessel:	n/a
26	chr7:97911938-97911988	Hepatocyte	liver:	n/a
27	chr7:97911390-97911440	RPTEC	kidney:	n/a
28	chr7:97911938-97911988	ovcar-3	ovarian:	n/a
29	chr7:97911512-97911562	AG10803	skin:	n/a
30	chr7:97910808-97910858	A549	lung:	n/a
31	chr7:97910878-97910928	Hepatocyte	liver:	n/a
32	chr7:97910884-97910934	SKMC	muscle:	n/a
33	chr7:97910884-97910934	AG10803	skin:	n/a
34	chr7:97910808-97910858	ECC-1	luminal epithelium:	n/a
35	chr7:97912149-97912199	A549	lung:	n/a
36	chr7:97911390-97911440	HAEpiC	amniotic membrane:	n/a
37	chr7:97911512-97911562	HIPEpiC	eye:	n/a
38	chr7:97912149-97912199	PANC-1	pancreas:	n/a
39	chr7:97910808-97910858	HEK293	kidney:	embryo
40	chr7:97910392-97910442	AG09319	gingival:	n/a
41	chr7:97911390-97911440	PFSK-1	brain:	n/a
42	chr7:97910870-97910920	HRPEpiC	eye:	n/a
43	chr7:97910884-97910934	SK-N-MC	brain:	n/a
44	chr7:97912149-97912199	GM12892	blood:	n/a
45	chr7:97910870-97910920	HAEpiC	amniotic membrane:	n/a
46	chr7:97911512-97911562	SAEC	small airway:	n/a
47	chr7:97910856-97910906	HUVEC	blood vessel:	n/a
48	chr7:97910856-97910906	GM12892	blood:	n/a
49	chr7:97910728-97910778	MCF-7	breast:	n/a
50	chr7:97910884-97910934	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97863932..97867672-chr7:97911936..97914933,4	K562	blood:
2	chr7:97907436..97910241-chr7:97949953..97951454,2	MCF-7	breast:
3	chr5:137673487..137674011-chr7:97910467..97911354,2	HCT-116	colon:
4	chr7:97880609..97882891-chr7:97909884..97913133,3	MCF-7	breast:
5	chr7:97880657..97883457-chr7:97908974..97910800,2	MCF-7	breast:
6	chr7:97900433..97904239-chr7:97908509..97910838,3	K562	blood:

Variant related genes	Relation type
BRI3	TF binding region
BRI3	CpG island
ENSG00000164713	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000120709	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11978420	chr7:97909193-97909194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182472848	chr7:97909205-97909206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs568317797	chr7:97909208-97909209	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535837741	chr7:97909256-97909257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs13238610	chr7:97909277-97909278	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs370123306	chr7:97909319-97909320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550437710	chr7:97909340-97909341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs575318210	chr7:97909357-97909358	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546014851	chr7:97909365-97909366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557043923	chr7:97909384-97909385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs573214509	chr7:97909390-97909391	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540528871	chr7:97909413-97909414	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113412734	chr7:97909468-97909469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs368059469	chr7:97909538-97909539	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs146496802	chr7:97909541-97909542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs71112135	chr7:97909548-97909549	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112929679	chr7:97909559-97909560	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs555543020	chr7:97909576-97909577	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs71112136	chr7:97909579-97909580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs529699386	chr7:97909636-97909637	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373405726	chr7:97909705-97909706	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144345781	chr7:97909739-97909740	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs575644712	chr7:97909758-97909759	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs541796280	chr7:97909792-97909793	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs148338972	chr7:97909795-97909796	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs375302864	chr7:97909808-97909809	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs530595450	chr7:97909949-97909950	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs186164198	chr7:97909950-97909951	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs191040450	chr7:97909951-97909952	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs577166704	chr7:97909994-97909995	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528392139	chr7:97910027-97910028	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs529912228	chr7:97910056-97910057	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs546624164	chr7:97910084-97910085	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs141587986	chr7:97910105-97910106	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs535514397	chr7:97910106-97910107	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs545896820	chr7:97910109-97910110	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs557301389	chr7:97910143-97910144	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs377473885	chr7:97910155-97910156	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs569029083	chr7:97910209-97910210	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs539511523	chr7:97910263-97910264	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs557937639	chr7:97910264-97910265	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573052310	chr7:97910277-97910278	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs540814553	chr7:97910318-97910319	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs147527442	chr7:97910327-97910328	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs548039209	chr7:97910341-97910342	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs574255727	chr7:97910350-97910351	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs367558899	chr7:97910361-97910362	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs370224881	chr7:97910377-97910378	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs181274586	chr7:97910453-97910454	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs563241787	chr7:97910454-97910455	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97886600-97909800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr7:97886800-97909200	Weak transcription	Brain Substantia Nigra	brain
3	chr7:97886800-97910000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:97887200-97910000	Weak transcription	Right Ventricle	heart
5	chr7:97887400-97910000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr7:97887600-97909600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:97891000-97909800	Weak transcription	Brain Hippocampus Middle	brain
8	chr7:97891000-97909800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:97891200-97909600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:97891200-97909800	Weak transcription	Aorta	Aorta
11	chr7:97891200-97909800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:97891400-97909600	Weak transcription	Primary B cells from cord blood	blood
13	chr7:97891400-97909800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr7:97892000-97909600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:97892000-97909800	Weak transcription	Spleen	Spleen
16	chr7:97892600-97909600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:97893400-97909200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:97895600-97910000	Weak transcription	HSMM	muscle
19	chr7:97895800-97909800	Weak transcription	Primary T cells from cord blood	blood
20	chr7:97895800-97910000	Weak transcription	Osteobl	bone
21	chr7:97896800-97909800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr7:97897000-97909800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:97903200-97909600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr7:97904600-97909600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:97906000-97910000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:97906000-97910000	Weak transcription	NHDF-Ad	bronchial
27	chr7:97906200-97909800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr7:97906200-97910000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:97906200-97910000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:97906200-97910000	Weak transcription	Fetal Lung	lung
31	chr7:97906200-97910000	Weak transcription	Ovary	ovary
32	chr7:97906400-97909600	Weak transcription	Fetal Intestine Large	intestine
33	chr7:97906400-97909800	Weak transcription	Colon Smooth Muscle	Colon
34	chr7:97906400-97910000	Weak transcription	Adipose Nuclei	Adipose
35	chr7:97906600-97909800	Weak transcription	Left Ventricle	heart
36	chr7:97907000-97909200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr7:97907400-97909600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr7:97907800-97909800	Enhancers	Placenta	Placenta
39	chr7:97907800-97910000	Enhancers	Pancreas	Pancrea
40	chr7:97907800-97910200	Enhancers	Stomach Mucosa	stomach
41	chr7:97908000-97909400	Enhancers	Gastric	stomach
42	chr7:97908000-97909600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:97908000-97909800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:97908200-97909800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr7:97908200-97909800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:97908200-97909800	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:97908200-97910000	Enhancers	Liver	Liver
48	chr7:97908400-97909200	Weak transcription	Colonic Mucosa	Colon
49	chr7:97908400-97909800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:97908400-97909800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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