Variant report

Variant	esv3409559
Chromosome Location	chr9:97135656-97138504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:97136408-97136810	K562	blood:	n/a	n/a
2	ATF3	chr9:97136437-97136651	K562	blood:	n/a	chr9:97136635-97136644 chr9:97136623-97136643
3	ATF3	chr9:97136451-97136657	HepG2	liver:	n/a	chr9:97136635-97136644 chr9:97136623-97136643
4	BATF	chr9:97138320-97138576	GM12878	blood:	n/a	n/a
5	BATF	chr9:97136440-97136776	GM12878	blood:	n/a	n/a
6	BATF	chr9:97138343-97138615	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:97136495-97136725	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:97138312-97138564	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:97138330-97138577	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:97137454-97137709	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:97136590-97136821	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:97136571-97136905	K562	blood:	n/a	chr9:97136834-97136850
13	BRCA1	chr9:97136553-97136781	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr9:97136369-97136913	K562	blood:	n/a	n/a
15	CBX3	chr9:97137432-97137777	K562	blood:	n/a	n/a
16	CBX3	chr9:97136409-97136799	K562	blood:	n/a	n/a
17	CCNT2	chr9:97136632-97137246	K562	blood:	n/a	n/a
18	CEBPB	chr9:97136454-97136744	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr9:97136443-97136566	K562	blood:	n/a	n/a
20	CEBPB	chr9:97137822-97137867	Hela-S3	cervix:	n/a	chr9:97137843-97137856
21	CEBPB	chr9:97137679-97137875	IMR90	lung:	n/a	chr9:97137843-97137856
22	CEBPB	chr9:97137668-97137868	K562	blood:	n/a	chr9:97137843-97137856
23	CEBPD	chr9:97136372-97137008	K562	blood:	n/a	n/a
24	CEBPD	chr9:97136686-97136904	HepG2	liver:	n/a	n/a
25	CHD2	chr9:97136542-97136795	GM12878	blood:	n/a	n/a
26	CHD2	chr9:97136546-97136909	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr9:97136680-97137007	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr9:97136528-97136995	K562	blood:	n/a	n/a
29	CREB1	chr9:97136551-97137015	HepG2	liver:	n/a	n/a
30	CREB1	chr9:97136434-97136765	A549	lung:	n/a	n/a
31	CREB1	chr9:97136442-97137059	A549	lung:	n/a	n/a
32	CREB1	chr9:97136539-97136849	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr9:97136530-97136998	GM12878	blood:	n/a	n/a
34	CTCF	chr9:97136639-97136747	Lung_OC	lung:	n/a	n/a
35	CTCF	chr9:97136715-97136748	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr9:97137556-97137597	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr9:97137583-97137652	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:97136679-97136684	Spleen_OC	spleen:	n/a	n/a
39	E2F4	chr9:97136421-97136944	MCF10A-Er-Src	breast:	n/a	chr9:97136779-97136789 chr9:97136780-97136790 chr9:97136797-97136806 chr9:97136630-97136642
40	E2F6	chr9:97137163-97137256	K562	blood:	n/a	chr9:97137216-97137225
41	E2F6	chr9:97136689-97136878	K562	blood:	n/a	chr9:97136779-97136789 chr9:97136780-97136790 chr9:97136797-97136806
42	EBF1	chr9:97136408-97137293	GM12878	blood:	n/a	n/a
43	EGR1	chr9:97136688-97136900	K562	blood:	n/a	chr9:97136797-97136807
44	ELF1	chr9:97136413-97136860	GM12878	blood:	n/a	n/a
45	ELF1	chr9:97137447-97137724	K562	blood:	n/a	n/a
46	ELF1	chr9:97136457-97136743	K562	blood:	n/a	n/a
47	ELF1	chr9:97136439-97136662	HepG2	liver:	n/a	n/a
48	ELF1	chr9:97136423-97136974	GM12878	blood:	n/a	n/a
49	ELF1	chr9:97136527-97136971	K562	blood:	n/a	n/a
50	ELF1	chr9:97137469-97137722	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:97136929-97136979	SK-N-MC	brain:	n/a
2	chr9:97136929-97136979	SK-N-MC	brain:	n/a
3	chr9:97136807-97136857	SKMC	muscle:	n/a
4	chr9:97137570-97137620	NHBE	bronchial:	n/a
5	chr9:97137570-97137620	ovcar-3	ovarian:	n/a
6	chr9:97136807-97136857	HCM	heart:	n/a
7	chr9:97136363-97136413	PANC-1	pancreas:	n/a
8	chr9:97136929-97136979	HNPCEpiC	eye:	n/a
9	chr9:97137570-97137620	BE2_C	brain:	n/a
10	chr9:97136929-97136979	GM06990	blood:	n/a
11	chr9:97136363-97136413	GM06990	blood:	n/a
12	chr9:97136929-97136979	PFSK-1	brain:	n/a
13	chr9:97136363-97136413	PFSK-1	brain:	n/a
14	chr9:97137570-97137620	K562	blood:	n/a
15	chr9:97136929-97136979	NT2-D1	testis:	n/a
16	chr9:97136363-97136413	MCF10A-Er-Src	breast:	n/a
17	chr9:97137570-97137620	SK-N-MC	brain:	n/a
18	chr9:97136363-97136413	GM12891	blood:	n/a
19	chr9:97136807-97136857	HNPCEpiC	eye:	n/a
20	chr9:97136807-97136857	HCT-116	colon:	n/a
21	chr9:97136807-97136857	K562	blood:	n/a
22	chr9:97136929-97136979	HRE	kidney:	n/a
23	chr9:97136929-97136979	HCF	heart:	n/a
24	chr9:97136807-97136857	CMK	blood:	n/a
25	chr9:97137570-97137620	NT2-D1	testis:	n/a
26	chr9:97137570-97137620	NH-A	brain:	n/a
27	chr9:97136363-97136413	A549	lung:	n/a
28	chr9:97137570-97137620	PFSK-1	brain:	n/a
29	chr9:97136807-97136857	T-47D	breast:	n/a
30	chr9:97136807-97136857	BE2_C	brain:	n/a
31	chr9:97136807-97136857	HUVEC	blood vessel:	n/a
32	chr9:97136929-97136979	BJ	skin:	n/a
33	chr9:97136929-97136979	ProgFib	skin:	n/a
34	chr9:97137570-97137620	NB4	blood:	n/a
35	chr9:97137570-97137620	U87	brain:	n/a
36	chr9:97136929-97136979	HIPEpiC	eye:	n/a
37	chr9:97137570-97137620	GM12891	blood:	n/a
38	chr9:97136807-97136857	NT2-D1	testis:	n/a
39	chr9:97136929-97136979	SK-N-SH_RA	brain:	n/a
40	chr9:97136929-97136979	HCT-116	colon:	n/a
41	chr9:97136363-97136413	GM12878	blood:	n/a
42	chr9:97136363-97136413	LNCaP	prostate:	n/a
43	chr9:97137570-97137620	NHDF-neo	bronchial:	n/a
44	chr9:97136363-97136413	HUVEC	blood vessel:	n/a
45	chr9:97137570-97137620	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:97136363-97136413	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:97137570-97137620	HEK293	kidney:	embryo
48	chr9:97136807-97136857	PrEC	prostate:	n/a
49	chr9:97136807-97136857	NHDF-neo	bronchial:	n/a
50	chr9:97136929-97136979	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:97135317..97137962-chr9:99774801..99776499,2	MCF-7	breast:
2	chr9:97137075..97138067-chr9:99774972..99775493,2	MCF-7	breast:

No data

Variant related genes	Relation type
HIATL1	TF binding region
HIATL1	CpG island
ENSG00000196312	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12343581	chr9:97135675-97135676	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs28702011	chr9:97135769-97135770	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556164509	chr9:97135800-97135801	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs28704121	chr9:97135905-97135906	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566476682	chr9:97135909-97135910	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545037793	chr9:97135922-97135923	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533765856	chr9:97135925-97135926	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558053424	chr9:97136025-97136026	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs111621411	chr9:97136049-97136050	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540431822	chr9:97136140-97136141	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs200060709	chr9:97136156-97136157	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375758348	chr9:97136157-97136158	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs9409744	chr9:97136160-97136161	Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs397834966	chr9:97136279-97136280	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189189813	chr9:97136307-97136308	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529045498	chr9:97136319-97136320	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544304685	chr9:97136320-97136321	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192122412	chr9:97136360-97136361	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532961502	chr9:97136363-97136364	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574542851	chr9:97136368-97136369	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs2987202	chr9:97136378-97136379	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs146118400	chr9:97136392-97136393	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs184168471	chr9:97136417-97136418	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs553605377	chr9:97136494-97136495	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs139259210	chr9:97136521-97136522	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190024467	chr9:97136550-97136551	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370397234	chr9:97136564-97136565	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567496060	chr9:97136573-97136574	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537981314	chr9:97136578-97136579	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549876392	chr9:97136581-97136582	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373101299	chr9:97136642-97136643	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571378322	chr9:97136695-97136696	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539026069	chr9:97136697-97136698	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12375475	chr9:97136733-97136734	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs142413498	chr9:97136820-97136821	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533842268	chr9:97136836-97136837	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555628760	chr9:97136850-97136851	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573865851	chr9:97136867-97136868	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544388960	chr9:97136877-97136878	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs3118796	chr9:97136884-97136885	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562596000	chr9:97136888-97136889	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577620645	chr9:97136945-97136946	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545001843	chr9:97136983-97136984	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2769724	chr9:97137078-97137079	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559886722	chr9:97137218-97137219	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528014498	chr9:97137245-97137246	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549246909	chr9:97137311-97137312	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112884759	chr9:97137333-97137334	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369161349	chr9:97137340-97137341	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531807765	chr9:97137354-97137355	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97136000-97136200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr9:97136000-97136200	Enhancers	Primary T cells fromperipheralblood	blood
3	chr9:97136000-97136200	Enhancers	Primary hematopoietic stem cells	blood
4	chr9:97136000-97137800	Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr9:97136000-97138000	Active TSS	Primary monocytes fromperipheralblood	blood
6	chr9:97136000-97138400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:97136200-97136400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr9:97136200-97136400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr9:97136200-97136600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr9:97136200-97136600	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr9:97136200-97136600	Active TSS	Primary T killer memory cells from peripheral blood	blood
12	chr9:97136200-97136600	Active TSS	Fetal Brain Male	brain
13	chr9:97136200-97136600	Active TSS	Fetal Heart	heart
14	chr9:97136200-97136600	Flanking Active TSS	Fetal Muscle Leg	muscle
15	chr9:97136200-97137000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr9:97136200-97137000	Active TSS	Brain Substantia Nigra	brain
17	chr9:97136200-97137800	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr9:97136200-97137800	Active TSS	Primary B cells from peripheral blood	blood
19	chr9:97136200-97137800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
20	chr9:97136200-97137800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr9:97136200-97137800	Active TSS	Brain Anterior Caudate	brain
22	chr9:97136200-97137800	Active TSS	Brain Hippocampus Middle	brain
23	chr9:97136200-97137800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:97136200-97137800	Active TSS	Colonic Mucosa	Colon
25	chr9:97136200-97137800	Active TSS	Placenta	Placenta
26	chr9:97136200-97137800	Active TSS	Ovary	ovary
27	chr9:97136200-97137800	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr9:97136200-97138000	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr9:97136200-97138000	Active TSS	H1 Cell Line	embryonic stem cell
30	chr9:97136200-97138000	Active TSS	H9 Cell Line	embryonic stem cell
31	chr9:97136200-97138000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:97136200-97138000	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr9:97136200-97138000	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr9:97136200-97138000	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr9:97136200-97138000	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr9:97136200-97138000	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr9:97136200-97138000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:97136200-97138000	Active TSS	Primary B cells from cord blood	blood
39	chr9:97136200-97138000	Active TSS	Primary T cells from cord blood	blood
40	chr9:97136200-97138000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr9:97136200-97138000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr9:97136200-97138000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr9:97136200-97138000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:97136200-97138000	Active TSS	Adipose Nuclei	Adipose
45	chr9:97136200-97138000	Active TSS	Liver	Liver
46	chr9:97136200-97138000	Active TSS	Brain Cingulate Gyrus	brain
47	chr9:97136200-97138000	Active TSS	Brain Germinal Matrix	brain
48	chr9:97136200-97138000	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr9:97136200-97138000	Active TSS	Colon Smooth Muscle	Colon
50	chr9:97136200-97138000	Active TSS	Duodenum Mucosa	Duodenum

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