Variant report

Variant	esv3339215
Chromosome Location	chr2:99550420-99554818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:135)
CpG islands
(count:796)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:135 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:99553086-99554164	H1-hESC	embryonic stem cell:	n/a	chr2:99554105-99554119
2	BRCA1	chr2:99553623-99553785	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr2:99553780-99553835	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr2:99553204-99553214	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr2:99552905-99553001	Lung_OC	lung:	n/a	n/a
6	CTCF	chr2:99552900-99553050	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr2:99552860-99553010	HEK293	kidney:	n/a	n/a
8	CTCF	chr2:99552940-99553090	SAEC	small airway:	n/a	n/a
9	CTCF	chr2:99552880-99553030	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr2:99552872-99553056	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr2:99552880-99553030	HMF	breast:	n/a	n/a
12	CTCF	chr2:99552920-99553070	GM12869	blood:	n/a	n/a
13	CTCF	chr2:99552763-99553145	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:99552880-99553030	AG09319	gingival:	n/a	n/a
15	CTCF	chr2:99552860-99553062	GM12891	blood:	n/a	n/a
16	CTCF	chr2:99552840-99552990	HA-sp	spinal cord:	n/a	n/a
17	CTCF	chr2:99552800-99552950	GM12865	blood:	n/a	n/a
18	CTCF	chr2:99552880-99553030	HEK293	kidney:	n/a	n/a
19	CTCF	chr2:99552847-99553064	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:99552897-99553013	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:99552885-99553033	GM19238	blood:	n/a	n/a
22	CTCF	chr2:99553020-99553170	HCT-116	colon:	n/a	n/a
23	CTCF	chr2:99552960-99553110	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr2:99552883-99553014	NHEK	skin:	n/a	n/a
25	CTCF	chr2:99552931-99553028	GM19240	blood:	n/a	n/a
26	CTCF	chr2:99552880-99553030	HL-60	blood:	n/a	n/a
27	CTCF	chr2:99552882-99553041	Gliobla	brain:	n/a	n/a
28	CTCF	chr2:99553060-99553210	HMEC	breast:	n/a	n/a
29	CTCF	chr2:99552846-99553033	HepG2	liver:	n/a	n/a
30	CTCF	chr2:99552880-99553030	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:99552960-99553110	GM12864	blood:	n/a	n/a
32	CTCF	chr2:99552877-99553051	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:99552780-99552930	A549	lung:	n/a	n/a
34	CTCF	chr2:99552870-99553048	GM12892	blood:	n/a	n/a
35	CTCF	chr2:99552860-99553010	HepG2	liver:	n/a	n/a
36	CTCF	chr2:99552880-99553030	RPTEC	kidney:	n/a	n/a
37	CTCF	chr2:99552940-99553090	GM12873	blood:	n/a	n/a
38	CTCF	chr2:99552920-99553070	GM12870	blood:	n/a	n/a
39	CTCF	chr2:99552900-99553050	HCT-116	colon:	n/a	n/a
40	CTCF	chr2:99552860-99553010	GM12866	blood:	n/a	n/a
41	CTCF	chr2:99552880-99553030	GM12871	blood:	n/a	n/a
42	CTCF	chr2:99552830-99553060	A549	lung:	n/a	n/a
43	CTCF	chr2:99552860-99553010	GM12869	blood:	n/a	n/a
44	CTCF	chr2:99552907-99552997	Fibrobl	skin:	n/a	n/a
45	CTCF	chr2:99552860-99553010	NB4	blood:	n/a	n/a
46	CTCF	chr2:99552880-99553030	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr2:99552880-99553030	HAc	cerebellar:	n/a	n/a
48	CTCF	chr2:99552960-99553110	GM12875	blood:	n/a	n/a
49	CTCF	chr2:99552880-99553030	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:99552903-99553035	SK-N-SH_RA	brain:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99553406-99553456	ProgFib	skin:	n/a
2	chr2:99552737-99552787	GM06990	blood:	n/a
3	chr2:99554416-99554466	HepG2	liver:	n/a
4	chr2:99553406-99553456	ProgFib	skin:	n/a
5	chr2:99552737-99552787	GM06990	blood:	n/a
6	chr2:99554416-99554466	HepG2	liver:	n/a
7	chr2:99552827-99552877	AoSMC	blood vessel:	n/a
8	chr2:99552633-99552683	IMR90	lung:	fetal
9	chr2:99553830-99553880	U87	brain:	n/a
10	chr2:99553642-99553692	NB4	blood:	n/a
11	chr2:99552261-99552311	HEEpiC	esophagus:	n/a
12	chr2:99553141-99553191	HCT-116	colon:	n/a
13	chr2:99553830-99553880	NHBE	bronchial:	n/a
14	chr2:99553406-99553456	T-47D	breast:	n/a
15	chr2:99552737-99552787	HIPEpiC	eye:	n/a
16	chr2:99552633-99552683	Hela-S3	cervix:	n/a
17	chr2:99553642-99553692	HCPEpiC	choroid plexus:	n/a
18	chr2:99552737-99552787	HCT-116	colon:	n/a
19	chr2:99553442-99553492	BE2_C	brain:	n/a
20	chr2:99553442-99553492	MCF-7	breast:	n/a
21	chr2:99553055-99553105	HCT-116	colon:	n/a
22	chr2:99553442-99553492	HRCEpiC	kidney:	n/a
23	chr2:99553830-99553880	H1-hESC	embryonic stem cell:	embryo
24	chr2:99553642-99553692	BE2_C	brain:	n/a
25	chr2:99553141-99553191	HEK293	kidney:	embryo
26	chr2:99553642-99553692	Caco-2	colon:	n/a
27	chr2:99552109-99552159	IMR90	lung:	fetal
28	chr2:99554416-99554466	HRPEpiC	eye:	n/a
29	chr2:99554416-99554466	NT2-D1	testis:	n/a
30	chr2:99552737-99552787	HUVEC	blood vessel:	n/a
31	chr2:99553078-99553128	Hepatocyte	liver:	n/a
32	chr2:99554416-99554466	GM19239	blood:	n/a
33	chr2:99553830-99553880	MCF10A-Er-Src	breast:	n/a
34	chr2:99552737-99552787	LNCaP	prostate:	n/a
35	chr2:99553078-99553128	Jurkat	blood:	n/a
36	chr2:99552109-99552159	HEK293	kidney:	embryo
37	chr2:99553078-99553128	HAEpiC	amniotic membrane:	n/a
38	chr2:99553078-99553128	MCF10A-Er-Src	breast:	n/a
39	chr2:99552827-99552877	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:99552737-99552787	HMEC	breast:	n/a
41	chr2:99553055-99553105	HAEpiC	amniotic membrane:	n/a
42	chr2:99552827-99552877	HepG2	liver:	n/a
43	chr2:99553442-99553492	RPTEC	kidney:	n/a
44	chr2:99553442-99553492	K562	blood:	n/a
45	chr2:99553078-99553128	MCF-7	breast:	n/a
46	chr2:99553406-99553456	HCT-116	colon:	n/a
47	chr2:99552261-99552311	NT2-D1	testis:	n/a
48	chr2:99553642-99553692	ECC-1	luminal epithelium:	n/a
49	chr2:99552633-99552683	ovcar-3	ovarian:	n/a
50	chr2:99553406-99553456	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:99523789..99526225-chr2:99550557..99552954,3	MCF-7	breast:

No data

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

Extended variants
information (count: 139 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:139 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570878909	chr2:99550422-99550423	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs186850207	chr2:99550428-99550429	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs371585463	chr2:99550430-99550431	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs112943047	chr2:99550454-99550455	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs546793598	chr2:99550468-99550469	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554476286	chr2:99550469-99550470	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs574659152	chr2:99550500-99550501	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563010526	chr2:99550513-99550514	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs534063108	chr2:99550548-99550549	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs369925514	chr2:99550563-99550564	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529894228	chr2:99550576-99550577	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576927029	chr2:99550595-99550596	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571086331	chr2:99550607-99550608	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373399022	chr2:99550659-99550660	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs397985273	chr2:99550679-99550680	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149389851	chr2:99550707-99550708	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs562569227	chr2:99550713-99550714	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576136213	chr2:99550779-99550780	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541833686	chr2:99550808-99550809	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561693640	chr2:99550886-99550887	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527999292	chr2:99550976-99550977	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548023327	chr2:99550977-99550978	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75039716	chr2:99551022-99551023	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533563982	chr2:99551046-99551047	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76519929	chr2:99551080-99551081	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529983432	chr2:99551151-99551152	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77716867	chr2:99551161-99551162	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535522633	chr2:99551287-99551288	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs76903795	chr2:99551369-99551370	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189734899	chr2:99551398-99551399	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533850553	chr2:99551442-99551443	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554023137	chr2:99551455-99551456	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570600246	chr2:99551493-99551494	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144674155	chr2:99551504-99551505	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77675236	chr2:99551513-99551514	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs72813046	chr2:99551531-99551532	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183890608	chr2:99551543-99551544	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188893969	chr2:99551599-99551600	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113707401	chr2:99551626-99551627	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555072056	chr2:99551676-99551677	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78610551	chr2:99551726-99551727	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113270845	chr2:99551728-99551729	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541403198	chr2:99551736-99551737	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13396750	chr2:99551739-99551740	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
45	rs537874889	chr2:99551744-99551745	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200137831	chr2:99551758-99551759	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs75227052	chr2:99551858-99551859	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543623864	chr2:99551966-99551967	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537490690	chr2:99552022-99552023	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549448390	chr2:99552031-99552032	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99538000-99550800	Weak transcription	Gastric	stomach
2	chr2:99538400-99551400	Weak transcription	Esophagus	oesophagus
3	chr2:99543800-99551200	Weak transcription	HMEC	breast
4	chr2:99543800-99551400	Weak transcription	Pancreas	Pancrea
5	chr2:99548600-99551200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:99549400-99553800	Active TSS	Brain Anterior Caudate	brain
7	chr2:99550000-99553800	Active TSS	Brain Angular Gyrus	brain
8	chr2:99550200-99550600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
9	chr2:99550400-99551400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:99550600-99551400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:99550800-99551000	Enhancers	Gastric	stomach
12	chr2:99550800-99553200	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr2:99551200-99551400	Enhancers	HMEC	breast
14	chr2:99551200-99553800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:99551200-99554000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr2:99551400-99551600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr2:99551400-99551600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:99551400-99551600	Enhancers	Pancreas	Pancrea
19	chr2:99551400-99551800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
20	chr2:99551400-99552000	Enhancers	Esophagus	oesophagus
21	chr2:99551400-99552000	Bivalent Enhancer	Fetal Brain Female	brain
22	chr2:99551400-99552000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr2:99551400-99552200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr2:99551400-99552200	Flanking Active TSS	HMEC	breast
25	chr2:99551400-99553800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
26	chr2:99551600-99551800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr2:99551600-99551800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
28	chr2:99551600-99551800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr2:99551600-99551800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr2:99551600-99551800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr2:99551600-99551800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:99551600-99551800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
33	chr2:99551600-99551800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:99551600-99551800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
35	chr2:99551600-99551800	Enhancers	Ovary	ovary
36	chr2:99551600-99551800	Flanking Active TSS	Pancreas	Pancrea
37	chr2:99551600-99552000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr2:99551600-99552000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:99551600-99552000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
40	chr2:99551600-99552000	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
41	chr2:99551600-99552000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:99551600-99552000	Bivalent Enhancer	Liver	Liver
43	chr2:99551600-99552000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr2:99551600-99552000	Bivalent Enhancer	HepG2	liver
45	chr2:99551600-99552200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr2:99551600-99552200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
47	chr2:99551600-99552200	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
48	chr2:99551600-99552200	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
49	chr2:99551600-99552200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
50	chr2:99551600-99552200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach

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