Variant report

Variant	esv3405434
Chromosome Location	chr9:102862531-102863979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:102863902-102864233	K562	blood:	n/a	n/a
2	BHLHE40	chr9:102863953-102864247	K562	blood:	n/a	n/a
3	CCNT2	chr9:102863942-102864235	K562	blood:	n/a	n/a
4	CEBPB	chr9:102861626-102862551	HepG2	liver:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
5	CEBPD	chr9:102863872-102864404	K562	blood:	n/a	n/a
6	CEBPD	chr9:102863811-102864280	K562	blood:	n/a	n/a
7	EP300	chr9:102862639-102862784	K562	blood:	n/a	n/a
8	EP300	chr9:102863870-102864247	K562	blood:	n/a	n/a
9	GABPA	chr9:102863917-102864215	K562	blood:	n/a	n/a
10	GATA1	chr9:102863907-102864233	PBDEFetal	blood:	n/a	n/a
11	GATA1	chr9:102863537-102864783	PBDE	blood:	n/a	n/a
12	GATA2	chr9:102863919-102864312	K562	blood:	n/a	n/a
13	GATA3	chr9:102863590-102863769	SH-SY5Y	brain:	n/a	n/a
14	HCFC1	chr9:102860073-102862658	Hela-S3	cervix:	n/a	n/a
15	HDAC2	chr9:102863914-102864222	K562	blood:	n/a	n/a
16	HDAC2	chr9:102863879-102864248	K562	blood:	n/a	n/a
17	HNF4A	chr9:102862601-102862804	HepG2	liver:	n/a	chr9:102862745-102862760 chr9:102862723-102862736 chr9:102862723-102862736 chr9:102862721-102862736 chr9:102862723-102862736 chr9:102862722-102862736 chr9:102862745-102862760 chr9:102862721-102862736 chr9:102862720-102862738 chr9:102862745-102862760 chr9:102862723-102862735 chr9:102862722-102862735
18	JUND	chr9:102863936-102864273	K562	blood:	n/a	n/a
19	MAX	chr9:102863943-102864184	K562	blood:	n/a	n/a
20	MXI1	chr9:102860222-102862815	IMR90	lung:	n/a	n/a
21	MYC	chr9:102863929-102864256	K562	blood:	n/a	n/a
22	MYC	chr9:102863922-102864276	K562	blood:	n/a	n/a
23	NR2F2	chr9:102863840-102864224	K562	blood:	n/a	n/a
24	POLR2A	chr9:102860314-102862580	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr9:102860270-102862684	GM12891	blood:	n/a	n/a
26	POLR2A	chr9:102863899-102864206	K562	blood:	n/a	n/a
27	POLR2A	chr9:102863523-102863700	HepG2	liver:	n/a	n/a
28	RCOR1	chr9:102863859-102864358	K562	blood:	n/a	n/a
29	RCOR1	chr9:102863886-102864343	K562	blood:	n/a	n/a
30	REST	chr9:102860286-102862685	H1-neurons	neurons:	n/a	n/a
31	STAT5A	chr9:102863798-102864346	K562	blood:	n/a	n/a
32	TAL1	chr9:102862640-102862675	K562	blood:	n/a	n/a
33	TAL1	chr9:102863710-102864311	K562	blood:	n/a	n/a
34	TBL1XR1	chr9:102863880-102864250	K562	blood:	n/a	n/a
35	TEAD4	chr9:102863783-102864356	K562	blood:	n/a	n/a
36	TEAD4	chr9:102863807-102864299	K562	blood:	n/a	n/a
37	ZMIZ1	chr9:102863908-102864273	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:102863959-102864009	SK-N-MC	brain:	n/a
2	chr9:102863959-102864009	HRPEpiC	eye:	n/a
3	chr9:102863959-102864009	A549	lung:	n/a
4	chr9:102863959-102864009	SAEC	small airway:	n/a
5	chr9:102863959-102864009	AoSMC	blood vessel:	n/a
6	chr9:102863959-102864009	MCF10A-Er-Src	breast:	n/a
7	chr9:102863959-102864009	SKMC	muscle:	n/a
8	chr9:102863959-102864009	HEEpiC	esophagus:	n/a
9	chr9:102863959-102864009	H1-hESC	embryonic stem cell:	embryo
10	chr9:102863959-102864009	T-47D	breast:	n/a
11	chr9:102863959-102864009	Jurkat	blood:	n/a
12	chr9:102863959-102864009	GM12891	blood:	n/a
13	chr9:102863959-102864009	Hepatocyte	liver:	n/a
14	chr9:102863959-102864009	HNPCEpiC	eye:	n/a
15	chr9:102863959-102864009	HIPEpiC	eye:	n/a
16	chr9:102863959-102864009	AG04449	skin:	fetal
17	chr9:102863959-102864009	K562	blood:	n/a
18	chr9:102863959-102864009	NHDF-neo	bronchial:	n/a
19	chr9:102863959-102864009	PFSK-1	brain:	n/a
20	chr9:102863959-102864009	HCPEpiC	choroid plexus:	n/a
21	chr9:102863959-102864009	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:102863959-102864009	ECC-1	luminal epithelium:	n/a
23	chr9:102863959-102864009	BE2_C	brain:	n/a
24	chr9:102863959-102864009	Caco-2	colon:	n/a
25	chr9:102863959-102864009	GM06990	blood:	n/a
26	chr9:102863959-102864009	BJ	skin:	n/a
27	chr9:102863959-102864009	HL-60	blood:	n/a
28	chr9:102863959-102864009	NH-A	brain:	n/a
29	chr9:102863959-102864009	HAEpiC	amniotic membrane:	n/a
30	chr9:102863959-102864009	AG04450	lung:	fetal
31	chr9:102863959-102864009	HUVEC	blood vessel:	n/a
32	chr9:102863959-102864009	PrEC	prostate:	n/a
33	chr9:102863959-102864009	SK-N-SH	brain:	n/a
34	chr9:102863959-102864009	HEK293	kidney:	embryo
35	chr9:102863959-102864009	HepG2	liver:	n/a
36	chr9:102863959-102864009	AG09319	gingival:	n/a
37	chr9:102863959-102864009	Hela-S3	cervix:	n/a
38	chr9:102863959-102864009	LNCaP	prostate:	n/a
39	chr9:102863959-102864009	HRE	kidney:	n/a
40	chr9:102863959-102864009	ProgFib	skin:	n/a
41	chr9:102863959-102864009	HCM	heart:	n/a
42	chr9:102863959-102864009	HMEC	breast:	n/a
43	chr9:102863959-102864009	SK-N-SH_RA	brain:	n/a
44	chr9:102863959-102864009	NHBE	bronchial:	n/a
45	chr9:102863959-102864009	NB4	blood:	n/a
46	chr9:102863959-102864009	AG10803	skin:	n/a
47	chr9:102863959-102864009	AG09309	skin:	n/a
48	chr9:102863959-102864009	GM12878	blood:	n/a
49	chr9:102863959-102864009	HCT-116	colon:	n/a
50	chr9:102863959-102864009	GM12892	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:102667836..102670748-chr9:102860445..102862735,2	K562	blood:
2	chr9:102861067..102864152-chr9:102881091..102884307,4	K562	blood:
3	chr15:45003558..45004176-chr9:102861994..102862803,2	Hela-S3	cervix:
4	chr9:102860210..102863951-chr9:102865614..102871017,5	K562	blood:
5	chr9:102581254..102583712-chr9:102860113..102863116,3	K562	blood:
6	chr9:102859693..102862029-chr9:102863024..102865040,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX17-2	chr9:102863583-102864299	NONHSAT133707

No data

Variant related genes	Relation type
ERP44	TF binding region
INVS	TF binding region
RN7SL75P	TF binding region
ERP44	CpG island
INVS	CpG island
RN7SL75P	CpG island
ENSG00000270995	chromatin interactions
ENSG00000237461	chromatin interactions
ENSG00000119509	chromatin interactions
ENSG00000023318	chromatin interactions
ENSG00000255145	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000136874	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10988972	chr9:102862539-102862540	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563368900	chr9:102862546-102862547	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs532630266	chr9:102862547-102862548	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs552350923	chr9:102862555-102862556	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs559800894	chr9:102862612-102862613	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs527467527	chr9:102862643-102862644	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs142061022	chr9:102862741-102862742	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs370437263	chr9:102862754-102862755	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs567554014	chr9:102862766-102862767	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs199529570	chr9:102862867-102862868	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs574259684	chr9:102862871-102862872	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200504352	chr9:102862878-102862879	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs59637286	chr9:102862881-102862882	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs549802070	chr9:102862882-102862883	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs569706638	chr9:102862886-102862887	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs538635515	chr9:102862899-102862900	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs71503729	chr9:102862905-102862906	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558318676	chr9:102862923-102862924	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs377177996	chr9:102862931-102862932	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs71370979	chr9:102862937-102862938	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs71498728	chr9:102862944-102862945	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs13288877	chr9:102862945-102862946	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs13293164	chr9:102862946-102862947	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs370614711	chr9:102862947-102862948	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs57032191	chr9:102862957-102862958	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs565786489	chr9:102862963-102862964	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs13288894	chr9:102862971-102862972	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558817741	chr9:102862972-102862973	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs34351574	chr9:102862973-102862974	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs67592817	chr9:102862978-102862979	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs376899033	chr9:102862983-102862984	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540643602	chr9:102862989-102862990	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534870867	chr9:102862994-102862995	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs13289036	chr9:102862997-102862998	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs574768803	chr9:102862998-102862999	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184660862	chr9:102863004-102863005	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371557613	chr9:102863007-102863008	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs543751620	chr9:102863021-102863022	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs557242373	chr9:102863022-102863023	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs188330080	chr9:102863028-102863029	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs191092583	chr9:102863031-102863032	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs373668902	chr9:102863037-102863038	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs13293358	chr9:102863044-102863045	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs184801386	chr9:102863045-102863046	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs189704883	chr9:102863046-102863047	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs574174976	chr9:102863051-102863052	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs13287290	chr9:102863052-102863053	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs374715780	chr9:102863055-102863056	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs13293367	chr9:102863059-102863060	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs13289068	chr9:102863060-102863061	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102859200-102862600	Active TSS	GM12878-XiMat	blood
2	chr9:102859200-102862600	Active TSS	K562	blood
3	chr9:102859600-102862800	Active TSS	NHLF	lung
4	chr9:102860000-102862600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:102860000-102862600	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr9:102860000-102862600	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr9:102860000-102862600	Active TSS	NHDF-Ad	bronchial
8	chr9:102860000-102862800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr9:102860000-102862800	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr9:102860200-102862600	Active TSS	Right Atrium	heart
11	chr9:102860200-102862600	Active TSS	A549	lung
12	chr9:102860200-102862800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:102860200-102862800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:102860200-102862800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr9:102860200-102862800	Active TSS	Right Ventricle	heart
16	chr9:102860400-102862600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:102860400-102862600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:102860400-102862600	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr9:102860400-102862600	Active TSS	HMEC	breast
20	chr9:102860400-102862800	Active TSS	Psoas Muscle	Psoas
21	chr9:102860600-102862600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr9:102860600-102862600	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr9:102860600-102862800	Active TSS	Hela-S3	cervix
24	chr9:102861000-102862600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:102861200-102862800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:102861600-102862600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr9:102861800-102862600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr9:102861800-102862600	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr9:102861800-102862800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:102862000-102862600	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr9:102862000-102862600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr9:102862000-102862600	Flanking Active TSS	Fetal Muscle Leg	muscle
33	chr9:102862000-102862600	Flanking Active TSS	NH-A	brain
34	chr9:102862000-102862600	Flanking Active TSS	Osteobl	bone
35	chr9:102862000-102862800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:102862000-102862800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:102862000-102862800	Flanking Active TSS	Fetal Brain Female	brain
38	chr9:102862000-102862800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr9:102862000-102862800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr9:102862000-102862800	Flanking Active TSS	HUVEC	blood vessel
41	chr9:102862200-102862600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:102862200-102862600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr9:102862200-102862600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:102862200-102862600	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr9:102862200-102862600	Flanking Active TSS	Fetal Stomach	stomach
46	chr9:102862200-102862800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:102862200-102862800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr9:102862200-102862800	Enhancers	Primary B cells from peripheral blood	blood
49	chr9:102862200-102862800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:102862200-102862800	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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