Variant report

Variant	esv2752334
Chromosome Location	chrX:74787887-75200415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:1100)
Chromatin interactive
region (count:7)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:74869144-74869552	HepG2	liver:	n/a	n/a
2	BACH1	chrX:74829387-74829454	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:74843276-74843446	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chrX:74961486-74961655	GM12878	blood:	n/a	n/a
5	BHLHE40	chrX:75183773-75183803	K562	blood:	n/a	n/a
6	BRCA1	chrX:74823696-74823895	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chrX:74823747-74823992	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chrX:74893266-74893618	HepG2	liver:	n/a	n/a
9	CEBPB	chrX:74919034-74919351	IMR90	lung:	n/a	n/a
10	CEBPB	chrX:75018254-75018442	A549	lung:	n/a	chrX:75018359-75018370
11	CEBPB	chrX:74919027-74919230	K562	blood:	n/a	n/a
12	CEBPB	chrX:74869775-74870061	HepG2	liver:	n/a	n/a
13	CEBPB	chrX:74893269-74893643	HepG2	liver:	n/a	n/a
14	CEBPB	chrX:74868673-74869415	HepG2	liver:	n/a	n/a
15	CEBPB	chrX:74869030-74869432	HepG2	liver:	n/a	n/a
16	CEBPB	chrX:75018210-75018528	HepG2	liver:	n/a	chrX:75018359-75018370
17	CEBPB	chrX:74915476-74915725	HepG2	liver:	n/a	chrX:74915614-74915625
18	CEBPB	chrX:75043526-75043671	IMR90	lung:	n/a	n/a
19	CEBPB	chrX:74893333-74893490	HepG2	liver:	n/a	n/a
20	CEBPB	chrX:74823767-74823964	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chrX:74823641-74823840	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chrX:74875495-74875812	HepG2	liver:	n/a	chrX:74875660-74875673
23	CEBPB	chrX:75083961-75084241	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:74804122-74804468	IMR90	lung:	n/a	chrX:74804291-74804302
25	CEBPB	chrX:74804127-74804455	HepG2	liver:	n/a	chrX:74804291-74804302
26	CEBPB	chrX:74966258-74966431	HepG2	liver:	n/a	n/a
27	CEBPB	chrX:74804116-74804454	K562	blood:	n/a	chrX:74804291-74804302
28	CEBPB	chrX:75060337-75060537	A549	lung:	n/a	n/a
29	CEBPB	chrX:74875570-74875783	MCF-7	breast:	n/a	chrX:74875660-74875673
30	CEBPB	chrX:74868752-74869399	HepG2	liver:	n/a	n/a
31	CEBPB	chrX:74865990-74866106	K562	blood:	n/a	n/a
32	CEBPB	chrX:74893337-74893663	HepG2	liver:	n/a	n/a
33	CEBPB	chrX:74915493-74915710	A549	lung:	n/a	chrX:74915614-74915625
34	CEBPB	chrX:74915587-74915704	IMR90	lung:	n/a	chrX:74915614-74915625
35	CEBPB	chrX:74869115-74869280	HepG2	liver:	n/a	n/a
36	CEBPD	chrX:75183636-75183981	K562	blood:	n/a	n/a
37	CEBPD	chrX:74869042-74869239	HepG2	liver:	n/a	n/a
38	CEBPD	chrX:74869033-74869316	HepG2	liver:	n/a	n/a
39	CHD1	chrX:75176331-75176337	GM12878	blood:	n/a	n/a
40	CREB1	chrX:74966947-74967222	GM12878	blood:	n/a	n/a
41	CREB1	chrX:74966820-74967220	HepG2	liver:	n/a	n/a
42	CREB1	chrX:74966883-74967280	HepG2	liver:	n/a	n/a
43	CREB1	chrX:74966951-74967171	A549	lung:	n/a	n/a
44	CTCF	chrX:74843481-74843609	HepG2	liver:	n/a	n/a
45	CTCF	chrX:75067060-75067210	GM06990	blood:	n/a	n/a
46	CTCF	chrX:74823785-74823965	GM10248	blood:	n/a	n/a
47	CTCF	chrX:74843500-74843650	HPAF	blood vessel:	n/a	n/a
48	CTCF	chrX:74823800-74823950	RPTEC	kidney:	n/a	n/a
49	CTCF	chrX:75107808-75107969	ProgFib	skin:	n/a	n/a
50	CTCF	chrX:74823760-74823910	SAEC	small airway:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:75006485-75006535	SAEC	small airway:	n/a
2	chrX:74963711-74963761	Caco-2	colon:	n/a
3	chrX:75006485-75006535	SAEC	small airway:	n/a
4	chrX:74963711-74963761	Caco-2	colon:	n/a
5	chrX:74963719-74963769	BJ	skin:	n/a
6	chrX:74963322-74963372	ovcar-3	ovarian:	n/a
7	chrX:75004943-75004993	SK-N-MC	brain:	n/a
8	chrX:75005096-75005146	HPAEpiC	pulmonary alveolar:	n/a
9	chrX:74962975-74963025	ProgFib	skin:	n/a
10	chrX:75006266-75006316	HRCEpiC	kidney:	n/a
11	chrX:75005102-75005152	AG09309	skin:	n/a
12	chrX:75004943-75004993	AG04450	lung:	fetal
13	chrX:75005096-75005146	ECC-1	luminal epithelium:	n/a
14	chrX:75005096-75005146	Hepatocyte	liver:	n/a
15	chrX:75005087-75005137	GM12878	blood:	n/a
16	chrX:75002912-75002962	HCF	heart:	n/a
17	chrX:75005087-75005137	AG04449	skin:	fetal
18	chrX:74963322-74963372	HAEpiC	amniotic membrane:	n/a
19	chrX:75004943-75004993	Jurkat	blood:	n/a
20	chrX:75005102-75005152	AoSMC	blood vessel:	n/a
21	chrX:75005028-75005078	GM19239	blood:	n/a
22	chrX:75005131-75005181	PFSK-1	brain:	n/a
23	chrX:75004943-75004993	HRPEpiC	eye:	n/a
24	chrX:75005087-75005137	NHDF-neo	bronchial:	n/a
25	chrX:74963322-74963372	SAEC	small airway:	n/a
26	chrX:75005096-75005146	GM12878	blood:	n/a
27	chrX:75006266-75006316	SAEC	small airway:	n/a
28	chrX:75005087-75005137	AG09309	skin:	n/a
29	chrX:74963719-74963769	AG10803	skin:	n/a
30	chrX:75005087-75005137	ovcar-3	ovarian:	n/a
31	chrX:75005131-75005181	SK-N-MC	brain:	n/a
32	chrX:75005028-75005078	GM06990	blood:	n/a
33	chrX:75005096-75005146	HMEC	breast:	n/a
34	chrX:75005096-75005146	NT2-D1	testis:	n/a
35	chrX:74965938-74965988	CMK	blood:	n/a
36	chrX:74966395-74966445	Hela-S3	cervix:	n/a
37	chrX:75004943-75004993	NH-A	brain:	n/a
38	chrX:74966395-74966445	RPTEC	kidney:	n/a
39	chrX:74966395-74966445	ovcar-3	ovarian:	n/a
40	chrX:75002912-75002962	AoSMC	blood vessel:	n/a
41	chrX:74966395-74966445	SK-N-SH	brain:	n/a
42	chrX:75005102-75005152	Jurkat	blood:	n/a
43	chrX:75006266-75006316	HEEpiC	esophagus:	n/a
44	chrX:74965938-74965988	ProgFib	skin:	n/a
45	chrX:75004943-75004993	CMK	blood:	n/a
46	chrX:75005096-75005146	HEK293	kidney:	embryo
47	chrX:75004943-75004993	BE2_C	brain:	n/a
48	chrX:75005360-75005410	HIPEpiC	eye:	n/a
49	chrX:75006266-75006316	Caco-2	colon:	n/a
50	chrX:74962975-74963025	U87	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:75187761..75188674-chrX:75347225..75347784,2	MCF-7	breast:
2	chrX:74964866..74967419-chrX:74972889..74974798,2	MCF-7	breast:
3	chrX:74055233..74056129-chrX:74823431..74824341,3	MCF-7	breast:
4	chrX:75035277..75036881-chrX:75164242..75166220,2	MCF-7	breast:
5	chrX:75003096..75005910-chrX:75006822..75008487,2	MCF-7	breast:
6	chrX:75035277..75036881-chrX:75164242..75166220,2	MCF-7	breast:
7	chrX:74956165..74958146-chrX:74961852..74964329,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXorf26-7	chrX:75040256-75041418	NONHSAT137665
2	lnc-CXorf26-7	chrX:75039665-75039735	NONHSAT137665
3	lnc-CXorf26-1	chrX:75123531-75124693	XLOC_008018
4	lnc-ZDHHC15-4	chrX:74856782-74858348	NONHSAT137662
5	lnc-CXorf26-2	chrX:75109183-75109872	NONHSAT137668
6	lnc-ZDHHC15-4	chrX:74868704-74869186	NONHSAT137662
7	lnc-CXorf26-2	chrX:75107994-75108278	ENSG00000230028.1
8	lnc-UPRT-5	chrX:74956007-74956890	NONHSAT137663
9	lnc-MAGEE2-2	chrX:74965904-74966749	NONHSAT137664
10	lnc-CXorf26-2	chrX:75108853-75109321	ENSG00000230028.1
11	lnc-ZDHHC15-4	chrX:74858763-74858953	NONHSAT137662
12	lnc-CXorf26-1	chrX:75122940-75123010	XLOC_008018

No data

Variant related genes	Relation type
ENSG00000226854	TF binding region
BRAFP1	TF binding region
SAR1AP4	TF binding region
ENSG00000226753	TF binding region
ENSG00000255752	TF binding region
TTC3P1	TF binding region
MAGEE2	TF binding region
ENSG00000226854	CpG island
BRAFP1	CpG island
SAR1AP4	CpG island
ENSG00000226753	CpG island
ENSG00000255752	CpG island
TTC3P1	CpG island
MAGEE2	CpG island
ENSG00000186675	chromatin interactions
ENSG00000215105	chromatin interactions

Extended variants
information (count: 2841 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:2841 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12559018	chrX:74787887-74787888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192179191	chrX:74787946-74787947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371269883	chrX:74788005-74788006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569578845	chrX:74788021-74788022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182534915	chrX:74788051-74788052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187327450	chrX:74788055-74788056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138272987	chrX:74788066-74788067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386417118	chrX:74788067-74788068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386417119	chrX:74788068-74788069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191420093	chrX:74788099-74788100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183894193	chrX:74788112-74788113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190578218	chrX:74788166-74788167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376792330	chrX:74788260-74788261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141805986	chrX:74788273-74788274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193034775	chrX:74788290-74788291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555578297	chrX:74788294-74788295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185770402	chrX:74788324-74788325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573889836	chrX:74788327-74788328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6647144	chrX:74788345-74788346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556626455	chrX:74788363-74788364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140554357	chrX:74788487-74788488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375296449	chrX:74788553-74788554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189798286	chrX:74788573-74788574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181575320	chrX:74788772-74788773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144398018	chrX:74788830-74788831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114858927	chrX:74788854-74788855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71853512	chrX:74788932-74788933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150058319	chrX:74788933-74788934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185424726	chrX:74788947-74788948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188718748	chrX:74788980-74788981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377035549	chrX:74789010-74789011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535945627	chrX:74789024-74789025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376568748	chrX:74789025-74789026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113527069	chrX:74789099-74789100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149790285	chrX:74789131-74789132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7053494	chrX:74789132-74789133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180758099	chrX:74789144-74789145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186082051	chrX:74789188-74789189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148925703	chrX:74789247-74789248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs5938109	chrX:74789301-74789302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191126267	chrX:74789360-74789361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374264433	chrX:74789398-74789399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370460130	chrX:74789415-74789416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374757666	chrX:74789417-74789418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368925934	chrX:74789470-74789471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183655173	chrX:74789479-74789480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57375601	chrX:74789545-74789546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57663710	chrX:74789564-74789565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35391142	chrX:74789568-74789569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7053969	chrX:74789622-74789623	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:47)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Lujan-Fryns syndrom	21572526	CNVD
Opitz-Kaveggia syndrome	21572526	CNVD
Cerebellar atrophy	21569638	CNVD
X-linked sideroblastic anemia	21569638	CNVD
Mental retardation	21572526	CNVD
ATR-X Syndrome	22470819	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Premature ovarian failure	20952765	CNVD
Pancreatic cancer	17952125	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:74786400-74805600	Weak transcription	Pancreas	Pancrea
2	chrX:74799200-74803400	Weak transcription	Brain Germinal Matrix	brain
3	chrX:74799800-74800200	ZNF genes & repeats	Ovary	ovary
4	chrX:74801600-74803000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chrX:74802800-74805000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chrX:74803000-74804200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chrX:74803200-74803800	ZNF genes & repeats	Fetal Brain Female	brain
8	chrX:74803400-74804000	ZNF genes & repeats	Brain Germinal Matrix	brain
9	chrX:74803600-74804200	ZNF genes & repeats	Ovary	ovary
10	chrX:74804200-74804400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chrX:74804200-74807600	Weak transcription	Ovary	ovary
12	chrX:74806200-74806400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chrX:74806400-74806600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
14	chrX:74816400-74816600	Enhancers	Colon Smooth Muscle	Colon
15	chrX:74823200-74823800	Enhancers	Fetal Kidney	kidney
16	chrX:74824000-74828000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chrX:74825600-74831600	Weak transcription	Ovary	ovary
18	chrX:74828000-74828800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chrX:74828400-74828800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chrX:74828400-74830400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chrX:74828600-74829000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chrX:74828600-74830000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chrX:74828600-74830200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chrX:74828800-74829800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chrX:74828800-74829800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chrX:74828800-74830200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chrX:74828800-74832000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chrX:74828800-74832800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chrX:74829000-74829200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chrX:74829000-74829800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chrX:74829000-74830000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chrX:74829200-74829400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chrX:74829200-74829800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chrX:74829400-74829600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chrX:74829600-74829800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chrX:74829800-74830800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chrX:74829800-74831000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chrX:74829800-74831200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chrX:74830000-74830200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chrX:74830000-74831000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chrX:74830200-74831000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chrX:74830200-74839800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chrX:74830800-74831000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chrX:74830800-74831800	Weak transcription	Aorta	Aorta
45	chrX:74831000-74831800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chrX:74831000-74831800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chrX:74831000-74831800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chrX:74831000-74831800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
49	chrX:74831200-74831400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chrX:74831600-74832600	ZNF genes & repeats	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links