Variant report

Variant	nsv529412
Chromosome Location	chrX:76711812-76957972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1041)
CpG islands
(count:122)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:76859117-76859830	HepG2	liver:	n/a	n/a
2	BATF	chrX:76896223-76896405	GM12878	blood:	n/a	chrX:76896340-76896351
3	BATF	chrX:76896163-76896505	GM12878	blood:	n/a	chrX:76896340-76896351
4	BCL3	chrX:76757473-76757813	GM12878	blood:	n/a	n/a
5	BHLHE40	chrX:76861103-76861111	GM12878	blood:	n/a	n/a
6	BHLHE40	chrX:76783204-76783727	K562	blood:	n/a	n/a
7	BRCA1	chrX:76820559-76820598	Hela-S3	cervix:	n/a	n/a
8	CBX3	chrX:76786757-76787011	K562	blood:	n/a	n/a
9	CBX3	chrX:76783099-76783483	K562	blood:	n/a	n/a
10	CBX3	chrX:76783571-76783845	K562	blood:	n/a	n/a
11	CCNT2	chrX:76711851-76712122	K562	blood:	n/a	n/a
12	CCNT2	chrX:76783174-76783715	K562	blood:	n/a	n/a
13	CEBPB	chrX:76782236-76783063	HepG2	liver:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
14	CEBPB	chrX:76888331-76888578	HepG2	liver:	n/a	chrX:76888331-76888348 chrX:76888415-76888426
15	CEBPB	chrX:76924422-76924728	K562	blood:	n/a	n/a
16	CEBPB	chrX:76856878-76856911	K562	blood:	n/a	n/a
17	CEBPB	chrX:76822382-76822673	HepG2	liver:	n/a	chrX:76822527-76822538
18	CEBPB	chrX:76782243-76783077	IMR90	lung:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
19	CEBPB	chrX:76782758-76783048	K562	blood:	n/a	chrX:76782904-76782915
20	CEBPB	chrX:76759163-76759200	A549	lung:	n/a	n/a
21	CEBPB	chrX:76762700-76762920	HepG2	liver:	n/a	chrX:76762780-76762791
22	CEBPB	chrX:76910983-76911274	IMR90	lung:	n/a	n/a
23	CEBPB	chrX:76760734-76761087	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:76782216-76783050	A549	lung:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
25	CEBPB	chrX:76924438-76924808	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chrX:76924457-76924769	IMR90	lung:	n/a	n/a
27	CEBPB	chrX:76822417-76822632	H1-hESC	embryonic stem cell:	n/a	chrX:76822527-76822538
28	CEBPB	chrX:76852179-76853000	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:76954931-76955085	HepG2	liver:	n/a	n/a
30	CEBPB	chrX:76715767-76716057	A549	lung:	n/a	n/a
31	CEBPB	chrX:76719465-76719685	HepG2	liver:	n/a	n/a
32	CEBPB	chrX:76782752-76783080	Hela-S3	cervix:	n/a	chrX:76782904-76782915
33	CEBPB	chrX:76924466-76924781	K562	blood:	n/a	n/a
34	CEBPB	chrX:76782215-76783425	K562	blood:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
35	CEBPB	chrX:76852730-76852876	A549	lung:	n/a	n/a
36	CEBPB	chrX:76822378-76822660	A549	lung:	n/a	chrX:76822527-76822538
37	CEBPB	chrX:76857453-76857668	HepG2	liver:	n/a	chrX:76857528-76857539
38	CEBPB	chrX:76782559-76783099	K562	blood:	n/a	chrX:76782904-76782915
39	CEBPB	chrX:76857403-76857655	IMR90	lung:	n/a	chrX:76857528-76857539
40	CEBPB	chrX:76822354-76822684	IMR90	lung:	n/a	chrX:76822527-76822538
41	CEBPB	chrX:76719457-76719741	IMR90	lung:	n/a	n/a
42	CEBPB	chrX:76715706-76716027	IMR90	lung:	n/a	n/a
43	CEBPB	chrX:76762653-76762919	A549	lung:	n/a	chrX:76762780-76762791
44	CEBPB	chrX:76762638-76762900	K562	blood:	n/a	chrX:76762780-76762791
45	CEBPB	chrX:76852201-76852999	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chrX:76715738-76716032	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chrX:76782744-76783031	H1-hESC	embryonic stem cell:	n/a	chrX:76782904-76782915
48	CEBPB	chrX:76786910-76786960	K562	blood:	n/a	n/a
49	CEBPB	chrX:76790904-76791369	Hela-S3	cervix:	n/a	chrX:76790907-76790920
50	CEBPB	chrX:76715765-76716031	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:76711903-76711953	AG09319	gingival:	n/a
2	chrX:76832207-76832257	CMK	blood:	n/a
3	chrX:76832207-76832257	HAEpiC	amniotic membrane:	n/a
4	chrX:76711903-76711953	PANC-1	pancreas:	n/a
5	chrX:76711903-76711953	HCT-116	colon:	n/a
6	chrX:76711903-76711953	HAEpiC	amniotic membrane:	n/a
7	chrX:76711903-76711953	HNPCEpiC	eye:	n/a
8	chrX:76711903-76711953	SAEC	small airway:	n/a
9	chrX:76832207-76832257	HRPEpiC	eye:	n/a
10	chrX:76832207-76832257	NB4	blood:	n/a
11	chrX:76711903-76711953	ProgFib	skin:	n/a
12	chrX:76711903-76711953	GM19239	blood:	n/a
13	chrX:76711903-76711953	GM12892	blood:	n/a
14	chrX:76711903-76711953	HRCEpiC	kidney:	n/a
15	chrX:76711903-76711953	T-47D	breast:	n/a
16	chrX:76832207-76832257	GM19239	blood:	n/a
17	chrX:76711903-76711953	GM12891	blood:	n/a
18	chrX:76711903-76711953	HEEpiC	esophagus:	n/a
19	chrX:76711903-76711953	A549	lung:	n/a
20	chrX:76711903-76711953	NHDF-neo	bronchial:	n/a
21	chrX:76711903-76711953	AG09309	skin:	n/a
22	chrX:76832207-76832257	SK-N-MC	brain:	n/a
23	chrX:76832207-76832257	Caco-2	colon:	n/a
24	chrX:76711903-76711953	PFSK-1	brain:	n/a
25	chrX:76832207-76832257	HCF	heart:	n/a
26	chrX:76832207-76832257	ovcar-3	ovarian:	n/a
27	chrX:76711903-76711953	HCPEpiC	choroid plexus:	n/a
28	chrX:76832207-76832257	Hepatocyte	liver:	n/a
29	chrX:76832207-76832257	AG10803	skin:	n/a
30	chrX:76832207-76832257	AG04450	lung:	fetal
31	chrX:76711903-76711953	HIPEpiC	eye:	n/a
32	chrX:76832207-76832257	H1-hESC	embryonic stem cell:	embryo
33	chrX:76832207-76832257	U87	brain:	n/a
34	chrX:76711903-76711953	RPTEC	kidney:	n/a
35	chrX:76832207-76832257	LNCaP	prostate:	n/a
36	chrX:76711903-76711953	BE2_C	brain:	n/a
37	chrX:76711903-76711953	HRPEpiC	eye:	n/a
38	chrX:76711903-76711953	AG04449	skin:	fetal
39	chrX:76711903-76711953	SK-N-SH_RA	brain:	n/a
40	chrX:76832207-76832257	HRCEpiC	kidney:	n/a
41	chrX:76832207-76832257	ProgFib	skin:	n/a
42	chrX:76711903-76711953	MCF-7	breast:	n/a
43	chrX:76832207-76832257	HUVEC	blood vessel:	n/a
44	chrX:76711903-76711953	H1-hESC	embryonic stem cell:	embryo
45	chrX:76832207-76832257	HepG2	liver:	n/a
46	chrX:76832207-76832257	HPAEpiC	pulmonary alveolar:	n/a
47	chrX:76711903-76711953	Jurkat	blood:	n/a
48	chrX:76832207-76832257	HEK293	kidney:	embryo
49	chrX:76711903-76711953	BJ	skin:	n/a
50	chrX:76711903-76711953	Hepatocyte	liver:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:76942261..76943831-chrX:76947036..76949639,2	MCF-7	breast:
2	chrX:76761448..76764250-chrX:76766493..76768451,2	MCF-7	breast:
3	chrX:76777436..76779959-chrX:76781784..76783298,2	K562	blood:
4	chrX:76889584..76891766-chrX:76894639..76897322,2	K562	blood:
5	chrX:76927289..76929660-chrX:76931892..76933429,2	MCF-7	breast:
6	chrX:76900558..76902843-chrX:76905942..76907892,2	MCF-7	breast:
7	chrX:76900558..76902843-chrX:76905942..76907892,2	MCF-7	breast:
8	chrX:76891482..76894301-chrX:76899024..76901296,2	MCF-7	breast:
9	chrX:76912843..76915064-chrX:76919242..76920879,2	K562	blood:
10	chrX:76884700..76887437-chrX:76888624..76890232,2	K562	blood:
11	chrX:76922852..76925730-chrX:76926707..76929215,2	K562	blood:
12	chrX:76912843..76915064-chrX:76919242..76920879,2	K562	blood:
13	chrX:76704759..76707077-chrX:76710548..76712188,2	MCF-7	breast:
14	chrX:76883999..76886686-chrX:76887036..76889742,2	K562	blood:
15	chrX:76926746..76928859-chrX:76931303..76934886,3	K562	blood:
16	chrX:76926746..76928859-chrX:76931303..76934886,3	K562	blood:
17	chrX:76927164..76929589-chrX:77151949..77154755,2	K562	blood:
18	chrX:76893077..76895046-chrX:77147729..77150138,2	MCF-7	breast:
19	chrX:76927289..76929660-chrX:76931892..76933429,2	MCF-7	breast:
20	chrX:76777436..76780005-chrX:76781673..76783298,3	K562	blood:
21	chrX:76890266..76892127-chrX:76895822..76897834,2	K562	blood:
22	chrX:76816472..76818842-chrX:76826313..76828243,2	K562	blood:
23	chr2:9877832..9879411-chrX:76718203..76719726,2	K562	blood:
24	chrX:76749546..76752499-chrX:76758608..76760224,2	K562	blood:
25	chrX:76916841..76919206-chrX:76922058..76924326,2	MCF-7	breast:
26	chrX:76883532..76887606-chrX:77150415..77153534,3	MCF-7	breast:
27	chrX:76800591..76802545-chrX:76807334..76809410,2	MCF-7	breast:
28	chrX:76848785..76850331-chrX:76854737..76856395,2	K562	blood:
29	chrX:76777436..76780005-chrX:76781673..76783298,3	K562	blood:
30	chrX:76853327..76855673-chrX:76856891..76859601,2	MCF-7	breast:
31	chrX:76853327..76855673-chrX:76856891..76859601,2	MCF-7	breast:
32	chrX:76916841..76919206-chrX:76922058..76924326,2	MCF-7	breast:
33	chrX:76816472..76818842-chrX:76826313..76828243,2	K562	blood:
34	chrX:76922852..76925730-chrX:76926707..76929215,2	K562	blood:
35	chrX:76761448..76764250-chrX:76766493..76768451,2	MCF-7	breast:
36	chrX:76942261..76943831-chrX:76947036..76949639,2	MCF-7	breast:
37	chrX:76800591..76802545-chrX:76807334..76809410,2	MCF-7	breast:
38	chrX:76950089..76952987-chrX:76954385..76957043,2	MCF-7	breast:
39	chrX:76950089..76952987-chrX:76954385..76957043,2	MCF-7	breast:
40	chrX:76749546..76752499-chrX:76758608..76760224,2	K562	blood:
41	chrX:76777436..76779959-chrX:76781784..76783298,2	K562	blood:
42	chrX:76884700..76887437-chrX:76888624..76890232,2	K562	blood:
43	chrX:76883999..76886686-chrX:76887036..76889742,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATRX	hsa-miR-30a-5p	chrX:76762578-76762600

Variant related genes	Relation type
ATRX	TF binding region
ATRX	CpG island
ENSG00000102158	chromatin interactions
ENSG00000085224	chromatin interactions

Extended variants
information (count: 2592 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:2592 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369332185	chrX:76711872-76711873	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373080668	chrX:76711900-76711901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375350173	chrX:76711904-76711905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs267606514	chrX:76711938-76711939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376606028	chrX:76711944-76711945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs41300245	chrX:76712314-76712315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79726844	chrX:76712398-76712399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35338449	chrX:76712530-76712531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28656769	chrX:76712698-76712699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368274846	chrX:76712777-76712778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189810830	chrX:76712903-76712904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181355690	chrX:76712969-76712970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146566356	chrX:76713073-76713074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371091099	chrX:76713169-76713170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111732970	chrX:76713192-76713193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533189512	chrX:76713241-76713242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551476436	chrX:76713351-76713352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184040095	chrX:76713380-76713381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188419363	chrX:76713392-76713393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375944235	chrX:76713508-76713509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180785273	chrX:76713535-76713536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187414541	chrX:76713624-76713625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192256199	chrX:76713699-76713700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181925184	chrX:76713747-76713748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28470727	chrX:76713750-76713751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200681153	chrX:76713788-76713789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371282641	chrX:76713795-76713796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187049535	chrX:76714030-76714031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28671049	chrX:76714156-76714157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143106711	chrX:76714160-76714161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190363990	chrX:76714162-76714163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371693115	chrX:76714252-76714253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182651815	chrX:76714454-76714455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148248397	chrX:76714461-76714462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141335333	chrX:76714567-76714568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567436942	chrX:76714644-76714645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75875536	chrX:76714671-76714672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76743462	chrX:76714672-76714673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534733146	chrX:76714673-76714674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199973645	chrX:76714757-76714758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201905411	chrX:76714820-76714821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367740332	chrX:76714821-76714822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150388137	chrX:76714864-76714865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186917070	chrX:76715066-76715067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367788175	chrX:76715085-76715086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549598229	chrX:76715163-76715164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137881679	chrX:76715183-76715184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189887770	chrX:76715225-76715226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371685680	chrX:76715264-76715265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375029007	chrX:76715414-76715415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

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
Breast cancer	21611746	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Alcoholism	21790672	CNVD
Mental retardation	22129561	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76705000-76713800	Weak transcription	Primary hematopoietic stem cells	blood
2	chrX:76709600-76713800	Weak transcription	Fetal Muscle Leg	muscle
3	chrX:76709600-76720400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chrX:76710600-76713000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chrX:76710600-76713200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chrX:76710800-76713200	Strong transcription	Fetal Muscle Trunk	muscle
7	chrX:76710800-76714400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chrX:76711200-76712000	Enhancers	Fetal Heart	heart
9	chrX:76713000-76721600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chrX:76713200-76714400	Weak transcription	Fetal Muscle Trunk	muscle
11	chrX:76713200-76715000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chrX:76747600-76749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chrX:76748600-76748800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chrX:76748600-76749000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chrX:76748600-76749000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chrX:76749000-76749200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chrX:76749000-76749200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chrX:76749000-76749200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chrX:76749000-76749800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chrX:76749200-76749400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chrX:76749200-76749400	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chrX:76749200-76749800	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chrX:76749200-76750000	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chrX:76749200-76750400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chrX:76749400-76749600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chrX:76749400-76749600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chrX:76749400-76749800	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chrX:76749400-76750000	Enhancers	NH-A	brain
29	chrX:76749400-76750200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chrX:76749400-76750200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chrX:76749400-76750200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chrX:76749400-76750200	Enhancers	Fetal Muscle Leg	muscle
33	chrX:76749400-76750200	Bivalent Enhancer	Placenta	Placenta
34	chrX:76749400-76750200	Enhancers	Hela-S3	cervix
35	chrX:76749400-76750200	Enhancers	HSMMtube	muscle
36	chrX:76749400-76750400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chrX:76749400-76750400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chrX:76749600-76749800	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chrX:76749600-76750000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chrX:76749600-76750000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chrX:76749600-76750000	Enhancers	Spleen	Spleen
42	chrX:76749600-76750200	Enhancers	H1 Cell Line	embryonic stem cell
43	chrX:76749800-76750000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chrX:76749800-76750200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chrX:76750000-76750200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chrX:76750000-76750200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chrX:76750200-76750400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chrX:76750200-76757000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chrX:76750200-76757600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chrX:76756400-76756600	Enhancers	Primary T helper naive cells from peripheral blood	blood

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