Variant report

Variant	nsv874697
Chromosome Location	chr2:99520608-99558970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:977)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99527778-99527986	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99525853-99526268	HepG2	liver:	n/a	n/a
3	BACH1	chr2:99553086-99554164	H1-hESC	embryonic stem cell:	n/a	chr2:99554105-99554119
4	BACH1	chr2:99540426-99540458	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:99528258-99528463	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:99553623-99553785	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:99527621-99528023	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:99541940-99542022	IMR90	lung:	n/a	chr2:99541942-99541953
9	CEBPB	chr2:99527682-99528001	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:99525735-99526149	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:99528964-99529550	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:99541847-99542083	HepG2	liver:	n/a	chr2:99541942-99541953
13	CEBPB	chr2:99527622-99528074	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:99527608-99528074	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:99541930-99542067	H1-hESC	embryonic stem cell:	n/a	chr2:99541942-99541953
16	CEBPB	chr2:99525859-99526248	HepG2	liver:	n/a	n/a
17	CHD1	chr2:99553780-99553835	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr2:99553204-99553214	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr2:99526016-99526315	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr2:99526049-99526225	HepG2	liver:	n/a	n/a
21	CREB1	chr2:99525911-99526214	A549	lung:	n/a	n/a
22	CREB1	chr2:99528862-99529364	A549	lung:	n/a	n/a
23	CTCF	chr2:99539883-99539944	GM13977	blood:	n/a	n/a
24	CTCF	chr2:99552870-99553048	GM12892	blood:	n/a	n/a
25	CTCF	chr2:99552880-99553030	A549	lung:	n/a	n/a
26	CTCF	chr2:99539840-99539990	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr2:99539800-99539950	GM12864	blood:	n/a	n/a
28	CTCF	chr2:99539800-99539950	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr2:99539764-99539990	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr2:99539910-99539994	LNCaP	prostate:	n/a	n/a
31	CTCF	chr2:99539800-99539950	WI-38	lung:	n/a	n/a
32	CTCF	chr2:99552883-99553014	NHEK	skin:	n/a	n/a
33	CTCF	chr2:99552860-99553010	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:99539778-99540039	IMR90	lung:	n/a	n/a
35	CTCF	chr2:99549670-99549674	HepG2	liver:	n/a	n/a
36	CTCF	chr2:99552880-99553030	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:99539871-99539947	GM12892	blood:	n/a	n/a
38	CTCF	chr2:99543763-99543778	K562	blood:	n/a	n/a
39	CTCF	chr2:99552940-99553090	GM12873	blood:	n/a	n/a
40	CTCF	chr2:99539800-99539950	HMEC	breast:	n/a	n/a
41	CTCF	chr2:99552885-99553033	GM19238	blood:	n/a	n/a
42	CTCF	chr2:99539840-99539990	GM12869	blood:	n/a	n/a
43	CTCF	chr2:99539817-99539990	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr2:99539880-99540030	HFF	foreskin:	n/a	n/a
45	CTCF	chr2:99527160-99527310	HepG2	liver:	n/a	n/a
46	CTCF	chr2:99553020-99553170	HCT-116	colon:	n/a	n/a
47	CTCF	chr2:99539860-99540010	GM12878	blood:	n/a	n/a
48	CTCF	chr2:99539820-99539970	GM12875	blood:	n/a	n/a
49	CTCF	chr2:99539880-99540030	SAEC	small airway:	n/a	n/a
50	CTCF	chr2:99552900-99553050	MCF-7	breast:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99553406-99553456	HCPEpiC	choroid plexus:	n/a
2	chr2:99553406-99553456	HCPEpiC	choroid plexus:	n/a
3	chr2:99536966-99537016	HCM	heart:	n/a
4	chr2:99552633-99552683	CMK	blood:	n/a
5	chr2:99553055-99553105	HEEpiC	esophagus:	n/a
6	chr2:99553830-99553880	Caco-2	colon:	n/a
7	chr2:99553830-99553880	A549	lung:	n/a
8	chr2:99554416-99554466	GM12891	blood:	n/a
9	chr2:99553406-99553456	HNPCEpiC	eye:	n/a
10	chr2:99553442-99553492	BE2_C	brain:	n/a
11	chr2:99553830-99553880	AG04449	skin:	fetal
12	chr2:99553055-99553105	HepG2	liver:	n/a
13	chr2:99554416-99554466	AG09309	skin:	n/a
14	chr2:99549050-99549100	AG04449	skin:	fetal
15	chr2:99526035-99526085	T-47D	breast:	n/a
16	chr2:99552109-99552159	PANC-1	pancreas:	n/a
17	chr2:99552633-99552683	GM19239	blood:	n/a
18	chr2:99553442-99553492	HEK293	kidney:	embryo
19	chr2:99553830-99553880	HEK293	kidney:	embryo
20	chr2:99552827-99552877	PrEC	prostate:	n/a
21	chr2:99553141-99553191	HUVEC	blood vessel:	n/a
22	chr2:99553141-99553191	AG09309	skin:	n/a
23	chr2:99552737-99552787	NHDF-neo	bronchial:	n/a
24	chr2:99553406-99553456	GM12891	blood:	n/a
25	chr2:99553642-99553692	HEK293	kidney:	embryo
26	chr2:99549050-99549100	PANC-1	pancreas:	n/a
27	chr2:99552827-99552877	HEK293	kidney:	embryo
28	chr2:99553642-99553692	SKMC	muscle:	n/a
29	chr2:99552737-99552787	SK-N-SH_RA	brain:	n/a
30	chr2:99552261-99552311	HEK293	kidney:	embryo
31	chr2:99553442-99553492	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:99552827-99552877	IMR90	lung:	fetal
33	chr2:99553642-99553692	NHDF-neo	bronchial:	n/a
34	chr2:99552109-99552159	HL-60	blood:	n/a
35	chr2:99552109-99552159	NH-A	brain:	n/a
36	chr2:99554416-99554466	HEK293	kidney:	embryo
37	chr2:99553141-99553191	HL-60	blood:	n/a
38	chr2:99553642-99553692	GM06990	blood:	n/a
39	chr2:99552633-99552683	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:99553830-99553880	AG09319	gingival:	n/a
41	chr2:99536966-99537016	HUVEC	blood vessel:	n/a
42	chr2:99553642-99553692	BE2_C	brain:	n/a
43	chr2:99553642-99553692	AG10803	skin:	n/a
44	chr2:99553406-99553456	HRE	kidney:	n/a
45	chr2:99553406-99553456	PFSK-1	brain:	n/a
46	chr2:99552633-99552683	HIPEpiC	eye:	n/a
47	chr2:99552737-99552787	AG09309	skin:	n/a
48	chr2:99526035-99526085	SK-N-SH_RA	brain:	n/a
49	chr2:99553141-99553191	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:99553406-99553456	ECC-1	luminal epithelium:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:99514144..99517054-chr2:99525112..99527785,2	MCF-7	breast:
2	chr2:99523789..99526225-chr2:99550557..99552954,3	MCF-7	breast:
3	chr2:99509338..99511041-chr2:99519600..99521247,2	MCF-7	breast:
4	chr2:99532387..99535858-chr2:99543640..99546629,3	MCF-7	breast:
5	chr2:99519571..99522164-chr2:99529112..99531136,2	MCF-7	breast:
6	chr2:99525536..99528520-chr2:99541090..99543085,2	MCF-7	breast:
7	chr2:99552279..99554160-chr2:99555590..99558457,2	MCF-7	breast:
8	chr2:99523325..99526612-chr2:99528163..99531065,4	K562	blood:
9	chr2:99528371..99530987-chr2:99533577..99536633,3	MCF-7	breast:
10	chr2:99525536..99528520-chr2:99541090..99543085,2	MCF-7	breast:
11	chr2:99484412..99487919-chr2:99523957..99528531,6	MCF-7	breast:
12	chr2:99532387..99535858-chr2:99543640..99546629,3	MCF-7	breast:
13	chr2:99523789..99526225-chr2:99550557..99552954,3	MCF-7	breast:
14	chr2:99528371..99530987-chr2:99533577..99536633,3	MCF-7	breast:
15	chr2:99519571..99522164-chr2:99529112..99531136,2	MCF-7	breast:
16	chr2:99551050..99554031-chr2:99555882..99558658,3	MCF-7	breast:
17	chr2:99536889..99540003-chr2:99549553..99553689,4	MCF-7	breast:
18	chr2:99496861..99499359-chr2:99536872..99539467,2	K562	blood:
19	chr2:99524391..99525989-chr2:99529125..99531065,2	K562	blood:
20	chr2:99524623..99526432-chr2:99530090..99532689,3	MCF-7	breast:

No data

Variant related genes	Relation type
KIAA1211L	TF binding region
KIAA1211L	CpG island
ENSG00000196872	chromatin interactions

Extended variants
information (count: 1389 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4851173	chr2:99520608-99520609	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557301943	chr2:99520617-99520618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141999092	chr2:99520659-99520660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542888418	chr2:99520670-99520671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553179538	chr2:99520736-99520737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572884423	chr2:99520789-99520790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112892633	chr2:99520808-99520809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564784696	chr2:99520829-99520830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530540513	chr2:99520861-99520862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144788998	chr2:99520869-99520870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561295233	chr2:99520870-99520871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191317121	chr2:99520908-99520909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565636896	chr2:99520926-99520927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546825384	chr2:99520969-99520970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371397812	chr2:99520978-99520979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184929342	chr2:99521010-99521011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147512865	chr2:99521018-99521019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140354875	chr2:99521033-99521034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569213893	chr2:99521073-99521074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116729525	chr2:99521099-99521100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554997795	chr2:99521101-99521102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567591738	chr2:99521110-99521111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536533147	chr2:99521117-99521118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536119684	chr2:99521120-99521121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371825801	chr2:99521206-99521207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189316766	chr2:99521215-99521216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572999704	chr2:99521246-99521247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554892884	chr2:99521275-99521276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374777165	chr2:99521297-99521298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554329396	chr2:99521304-99521305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558661855	chr2:99521333-99521334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144358601	chr2:99521343-99521344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192499214	chr2:99521345-99521346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113536825	chr2:99521351-99521352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4850889	chr2:99521385-99521386	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs185482231	chr2:99521387-99521388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529608887	chr2:99521496-99521497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111959417	chr2:99521569-99521570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35679246	chr2:99521606-99521607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533744339	chr2:99521629-99521630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560577063	chr2:99521637-99521638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532749329	chr2:99521664-99521665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552484669	chr2:99521691-99521692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181426474	chr2:99521692-99521693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369498076	chr2:99521712-99521713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72813029	chr2:99521728-99521729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531816489	chr2:99521742-99521743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145457148	chr2:99521779-99521780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576834338	chr2:99521781-99521782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568478088	chr2:99521791-99521792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99512000-99526000	Weak transcription	Right Atrium	heart
2	chr2:99513200-99525000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:99515200-99524600	Weak transcription	Pancreas	Pancrea
4	chr2:99517600-99526000	Weak transcription	Gastric	stomach
5	chr2:99518800-99525000	Weak transcription	Spleen	Spleen
6	chr2:99519600-99524800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:99520400-99521000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:99520400-99521000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:99520400-99522400	Weak transcription	Fetal Brain Male	brain
10	chr2:99520600-99520800	Enhancers	Brain Cingulate Gyrus	brain
11	chr2:99520600-99521000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:99520600-99521000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr2:99520600-99521000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:99520600-99521000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr2:99520600-99521400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr2:99520800-99521000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:99520800-99528600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr2:99521000-99525000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:99521000-99525000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:99521000-99525000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:99521000-99525200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr2:99521000-99526000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:99523800-99525600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr2:99523800-99526000	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:99523800-99526600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:99523800-99526800	Enhancers	Esophagus	oesophagus
27	chr2:99523800-99530000	Enhancers	Fetal Muscle Leg	muscle
28	chr2:99524000-99524200	Enhancers	Fetal Brain Female	brain
29	chr2:99524000-99525600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr2:99524000-99525800	Enhancers	Brain Angular Gyrus	brain
31	chr2:99524000-99526200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:99524400-99525400	Enhancers	Fetal Muscle Trunk	muscle
33	chr2:99524400-99525800	Weak transcription	Fetal Brain Female	brain
34	chr2:99524400-99525800	Enhancers	HUVEC	blood vessel
35	chr2:99524400-99526600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:99524400-99528400	Enhancers	HMEC	breast
37	chr2:99524400-99534400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:99524600-99526000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr2:99524600-99526600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:99524600-99526600	Enhancers	Stomach Mucosa	stomach
41	chr2:99524600-99526800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:99524600-99526800	Enhancers	NHEK	skin
43	chr2:99524600-99532400	Enhancers	Pancreas	Pancrea
44	chr2:99524800-99525000	Enhancers	Brain Hippocampus Middle	brain
45	chr2:99524800-99525000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:99524800-99525200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:99524800-99525200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:99524800-99525200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr2:99524800-99525400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:99524800-99525400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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