Variant report

Variant	esv3330996
Chromosome Location	chr9:98083446-98112507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:443)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:98111306-98111727	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:98112151-98112338	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:98083859-98084280	IMR90	lung:	n/a	chr9:98084194-98084205
4	CEBPB	chr9:98107111-98107581	A549	lung:	n/a	chr9:98107418-98107429
5	CEBPB	chr9:98095804-98096055	Hela-S3	cervix:	n/a	chr9:98095896-98095909 chr9:98095897-98095908
6	CEBPB	chr9:98095836-98096036	HepG2	liver:	n/a	chr9:98095896-98095909 chr9:98095897-98095908
7	CEBPB	chr9:98103008-98103328	HepG2	liver:	n/a	chr9:98103143-98103154
8	CEBPB	chr9:98107006-98107577	Hela-S3	cervix:	n/a	chr9:98107418-98107429
9	CEBPB	chr9:98103027-98103289	K562	blood:	n/a	chr9:98103143-98103154
10	CEBPB	chr9:98107095-98107486	K562	blood:	n/a	chr9:98107418-98107429
11	CEBPB	chr9:98107066-98107575	IMR90	lung:	n/a	chr9:98107418-98107429
12	CEBPB	chr9:98103059-98103295	A549	lung:	n/a	chr9:98103143-98103154
13	CEBPB	chr9:98103031-98103285	IMR90	lung:	n/a	chr9:98103143-98103154
14	CEBPB	chr9:98107005-98107580	HepG2	liver:	n/a	chr9:98107418-98107429
15	CEBPB	chr9:98083914-98084377	HepG2	liver:	n/a	chr9:98084194-98084205
16	CEBPZ	chr9:98089694-98089857	HepG2	liver:	n/a	n/a
17	CHD1	chr9:98103798-98103820	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr9:98111283-98112727	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:98098680-98098830	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:98098612-98098955	A549	lung:	n/a	n/a
21	CTCF	chr9:98098702-98098846	LNCaP	prostate:	n/a	n/a
22	CTCF	chr9:98104000-98104150	GM12871	blood:	n/a	n/a
23	CTCF	chr9:98098707-98098870	GM19239	blood:	n/a	n/a
24	CTCF	chr9:98098780-98098930	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr9:98098700-98098850	HCFaa	heart:	n/a	n/a
26	CTCF	chr9:98104048-98104149	GM19240	blood:	n/a	n/a
27	CTCF	chr9:98104000-98104150	SAEC	small airway:	n/a	n/a
28	CTCF	chr9:98098740-98098890	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr9:98104020-98104170	AG10803	skin:	n/a	n/a
30	CTCF	chr9:98098660-98098810	HRE	kidney:	n/a	n/a
31	CTCF	chr9:98098760-98098910	HVMF	connective:	n/a	n/a
32	CTCF	chr9:98104046-98104143	GM12891	blood:	n/a	n/a
33	CTCF	chr9:98086781-98086848	GM13976	blood:	n/a	n/a
34	CTCF	chr9:98098740-98098890	GM12873	blood:	n/a	n/a
35	CTCF	chr9:98098720-98098870	K562	blood:	n/a	n/a
36	CTCF	chr9:98098720-98098870	HMF	breast:	n/a	n/a
37	CTCF	chr9:98098660-98098810	GM12864	blood:	n/a	n/a
38	CTCF	chr9:98098680-98098830	RPTEC	kidney:	n/a	n/a
39	CTCF	chr9:98098680-98098830	A549	lung:	n/a	n/a
40	CTCF	chr9:98104020-98104170	AG04450	lung:	n/a	n/a
41	CTCF	chr9:98098700-98098850	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr9:98104020-98104170	BE2_C	brain:	n/a	n/a
43	CTCF	chr9:98104016-98104169	GM12892	blood:	n/a	n/a
44	CTCF	chr9:98104000-98104150	HVMF	connective:	n/a	n/a
45	CTCF	chr9:98098700-98098850	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr9:98104020-98104170	HMF	breast:	n/a	n/a
47	CTCF	chr9:98098643-98098846	HepG2	liver:	n/a	n/a
48	CTCF	chr9:98098692-98098896	ProgFib	skin:	n/a	n/a
49	CTCF	chr9:98107060-98107210	GM12869	blood:	n/a	n/a
50	CTCF	chr9:98104002-98104207	SK-N-SH_RA	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98112381-98112431	Caco-2	colon:	n/a
2	chr9:98109802-98109852	LNCaP	prostate:	n/a
3	chr9:98112381-98112431	HepG2	liver:	n/a
4	chr9:98111365-98111415	HIPEpiC	eye:	n/a
5	chr9:98112381-98112431	NH-A	brain:	n/a
6	chr9:98111970-98112020	AG04449	skin:	fetal
7	chr9:98111970-98112020	GM12891	blood:	n/a
8	chr9:98111365-98111415	K562	blood:	n/a
9	chr9:98112381-98112431	HL-60	blood:	n/a
10	chr9:98111365-98111415	GM12878	blood:	n/a
11	chr9:98112381-98112431	SKMC	muscle:	n/a
12	chr9:98112381-98112431	HCF	heart:	n/a
13	chr9:98112381-98112431	PrEC	prostate:	n/a
14	chr9:98111970-98112020	Hela-S3	cervix:	n/a
15	chr9:98111365-98111415	HEK293	kidney:	embryo
16	chr9:98112381-98112431	AoSMC	blood vessel:	n/a
17	chr9:98109802-98109852	ovcar-3	ovarian:	n/a
18	chr9:98109802-98109852	NHBE	bronchial:	n/a
19	chr9:98112381-98112431	GM12878	blood:	n/a
20	chr9:98109802-98109852	HRPEpiC	eye:	n/a
21	chr9:98112381-98112431	NB4	blood:	n/a
22	chr9:98111970-98112020	HRPEpiC	eye:	n/a
23	chr9:98111970-98112020	SAEC	small airway:	n/a
24	chr9:98109802-98109852	GM12891	blood:	n/a
25	chr9:98111970-98112020	H1-hESC	embryonic stem cell:	embryo
26	chr9:98111365-98111415	HCM	heart:	n/a
27	chr9:98111970-98112020	HPAEpiC	pulmonary alveolar:	n/a
28	chr9:98111970-98112020	Caco-2	colon:	n/a
29	chr9:98111970-98112020	NH-A	brain:	n/a
30	chr9:98109802-98109852	Jurkat	blood:	n/a
31	chr9:98112381-98112431	SK-N-MC	brain:	n/a
32	chr9:98111970-98112020	HNPCEpiC	eye:	n/a
33	chr9:98111365-98111415	HEEpiC	esophagus:	n/a
34	chr9:98112381-98112431	BE2_C	brain:	n/a
35	chr9:98109802-98109852	Caco-2	colon:	n/a
36	chr9:98111970-98112020	SK-N-SH	brain:	n/a
37	chr9:98111365-98111415	HCF	heart:	n/a
38	chr9:98111365-98111415	ovcar-3	ovarian:	n/a
39	chr9:98112381-98112431	PANC-1	pancreas:	n/a
40	chr9:98112381-98112431	HEK293	kidney:	embryo
41	chr9:98109802-98109852	HCPEpiC	choroid plexus:	n/a
42	chr9:98112381-98112431	ProgFib	skin:	n/a
43	chr9:98111970-98112020	IMR90	lung:	fetal
44	chr9:98112381-98112431	H1-hESC	embryonic stem cell:	embryo
45	chr9:98109802-98109852	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:98111970-98112020	BE2_C	brain:	n/a
47	chr9:98112381-98112431	NT2-D1	testis:	n/a
48	chr9:98111365-98111415	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:98111365-98111415	Hela-S3	cervix:	n/a
50	chr9:98112381-98112431	HCPEpiC	choroid plexus:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:98091823..98093994-chr9:98273200..98274710,2	MCF-7	breast:
2	chr9:98103672..98105349-chr9:98272991..98274766,2	K562	blood:
3	chr9:98079643..98081952-chr9:98093739..98095261,2	K562	blood:
4	chr9:98105856..98107591-chr9:98107862..98110752,2	MCF-7	breast:
5	chr9:98108850..98111338-chr9:98112509..98115346,2	K562	blood:
6	chr9:98110078..98112220-chr9:98115357..98117832,2	K562	blood:
7	chr9:98079065..98081246-chr9:98081282..98084712,4	MCF-7	breast:
8	chr9:98112082..98114768-chr9:98116884..98119446,2	K562	blood:
9	chr9:98103822..98104598-chr9:98336133..98336924,2	MCF-7	breast:
10	chr9:98079075..98081701-chr9:98084998..98086597,2	MCF-7	breast:
11	chr9:98087444..98089027-chr9:98092636..98095635,2	MCF-7	breast:
12	chr9:98077863..98081440-chr9:98083257..98086421,5	K562	blood:
13	chr9:98073006..98075860-chr9:98082691..98086114,3	K562	blood:
14	chr9:98103117..98105950-chr9:98116720..98118774,2	MCF-7	breast:
15	chr9:98103184..98105330-chr9:98187683..98189583,2	MCF-7	breast:
16	chr9:98081819..98084484-chr9:98117937..98119790,2	MCF-7	breast:
17	chr9:98087444..98089027-chr9:98092636..98095635,2	MCF-7	breast:
18	chr9:98105856..98107591-chr9:98107862..98110752,2	MCF-7	breast:
19	chr9:98104888..98106927-chr9:98272777..98274676,2	MCF-7	breast:

No data

Variant related genes	Relation type
FANCC	TF binding region
FANCC	CpG island
ENSG00000237857	chromatin interactions
ENSG00000158169	chromatin interactions

Extended variants
information (count: 785 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:785 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558808328	chr9:98083450-98083451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576938587	chr9:98083465-98083466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534951873	chr9:98083614-98083615	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552990714	chr9:98083648-98083649	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199939222	chr9:98083712-98083713	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574630551	chr9:98083723-98083724	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530922424	chr9:98083751-98083752	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549139070	chr9:98083791-98083792	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140172873	chr9:98083901-98083902	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576153875	chr9:98083966-98083967	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543491315	chr9:98083981-98083982	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs565510940	chr9:98083998-98083999	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs118115390	chr9:98083999-98084000	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184574227	chr9:98084016-98084017	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559795767	chr9:98084029-98084030	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149782512	chr9:98084073-98084074	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189046810	chr9:98084089-98084090	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201071429	chr9:98084106-98084107	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75903834	chr9:98084108-98084109	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77450722	chr9:98084126-98084127	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182546342	chr9:98084148-98084149	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552284698	chr9:98084149-98084150	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570673541	chr9:98084151-98084152	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs186173234	chr9:98084153-98084154	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs144676937	chr9:98084208-98084209	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs189121802	chr9:98084255-98084256	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369554105	chr9:98084256-98084257	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554574496	chr9:98084327-98084328	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373719271	chr9:98084340-98084341	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs78115144	chr9:98084366-98084367	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543552795	chr9:98084385-98084386	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548392879	chr9:98084403-98084404	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371392000	chr9:98084487-98084488	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs547146101	chr9:98084491-98084492	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571511834	chr9:98084504-98084505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577218959	chr9:98084547-98084548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539105211	chr9:98084663-98084664	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541272702	chr9:98084670-98084671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559861273	chr9:98084711-98084712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530437531	chr9:98084719-98084720	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562116361	chr9:98084749-98084750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563306895	chr9:98084906-98084907	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78205806	chr9:98084909-98084910	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569460705	chr9:98084910-98084911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374824816	chr9:98084966-98084967	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552156351	chr9:98084992-98084993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570463436	chr9:98085063-98085064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537027370	chr9:98085071-98085072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs569716037	chr9:98085119-98085120	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528155703	chr9:98085180-98085181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98080400-98083600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:98080600-98083600	Weak transcription	Fetal Lung	lung
3	chr9:98080600-98083600	Weak transcription	HMEC	breast
4	chr9:98080600-98083600	Weak transcription	NHEK	skin
5	chr9:98080600-98083800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:98080800-98083600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:98082200-98084200	Enhancers	HepG2	liver
8	chr9:98083200-98083600	Enhancers	Fetal Intestine Large	intestine
9	chr9:98083200-98083800	Enhancers	Adipose Nuclei	Adipose
10	chr9:98083400-98084000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr9:98083600-98084000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:98083600-98084000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:98083600-98084000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:98083600-98084000	Enhancers	Fetal Lung	lung
15	chr9:98083600-98084200	Enhancers	HMEC	breast
16	chr9:98083600-98084400	Enhancers	NHEK	skin
17	chr9:98083800-98084000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:98083800-98084400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr9:98087800-98089400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:98091000-98092800	Enhancers	HepG2	liver
21	chr9:98092800-98093600	Flanking Active TSS	HepG2	liver
22	chr9:98093600-98093800	Enhancers	HepG2	liver
23	chr9:98093800-98095400	Weak transcription	HepG2	liver
24	chr9:98095200-98095400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr9:98095200-98095600	Enhancers	Adipose Nuclei	Adipose
26	chr9:98095400-98095800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:98095400-98096000	Enhancers	HepG2	liver
28	chr9:98095600-98095800	Enhancers	Hela-S3	cervix
29	chr9:98095600-98096200	Enhancers	Fetal Lung	lung
30	chr9:98095800-98096600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:98096000-98097200	Weak transcription	Hela-S3	cervix
32	chr9:98096000-98098400	Weak transcription	HepG2	liver
33	chr9:98096200-98097600	Weak transcription	Fetal Lung	lung
34	chr9:98096600-98098400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:98097200-98098200	Enhancers	Hela-S3	cervix
36	chr9:98097600-98097800	Enhancers	Fetal Lung	lung
37	chr9:98097800-98098400	Weak transcription	Fetal Lung	lung
38	chr9:98098400-98098600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:98098400-98099000	Enhancers	Fetal Lung	lung
40	chr9:98098400-98099200	Enhancers	HepG2	liver
41	chr9:98099000-98102600	Weak transcription	Fetal Lung	lung
42	chr9:98099200-98099400	Bivalent Enhancer	HepG2	liver
43	chr9:98099200-98099600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr9:98099200-98101000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:98099400-98100800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:98099600-98105000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr9:98100200-98101000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:98101000-98105000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:98102600-98104200	Enhancers	Fetal Lung	lung
50	chr9:98103200-98104200	Enhancers	Fetal Stomach	stomach

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