Variant report

Variant	esv3369442
Chromosome Location	chrX:76969046-77309072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3636)
CpG islands
(count:3055)
Chromatin interactive
region (count:91)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:3636 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:77154600-77155313	K562	blood:	n/a	n/a
2	ARID3A	chrX:77193422-77194139	K562	blood:	n/a	n/a
3	ARID3A	chrX:77154591-77155133	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:77041605-77042036	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:77192650-77193220	K562	blood:	n/a	n/a
6	ARID3A	chrX:77043457-77043765	HepG2	liver:	n/a	n/a
7	ARID3A	chrX:77178130-77178731	K562	blood:	n/a	n/a
8	ARID3A	chrX:77042335-77042860	HepG2	liver:	n/a	n/a
9	ARID3A	chrX:77198895-77198941	K562	blood:	n/a	n/a
10	ARID3A	chrX:77151002-77151189	K562	blood:	n/a	n/a
11	ARID3A	chrX:77285171-77285468	K562	blood:	n/a	n/a
12	ARID3A	chrX:77165841-77166455	HepG2	liver:	n/a	n/a
13	ARID3A	chrX:77208676-77209085	K562	blood:	n/a	n/a
14	ARID3A	chrX:77179946-77180187	K562	blood:	n/a	n/a
15	ARID3A	chrX:77150768-77151408	HepG2	liver:	n/a	n/a
16	ATF1	chrX:77154596-77155174	K562	blood:	n/a	n/a
17	ATF1	chrX:77150539-77151358	K562	blood:	n/a	n/a
18	ATF1	chrX:77041653-77042058	K562	blood:	n/a	chrX:77041828-77041842
19	ATF2	chrX:77154483-77155156	GM12878	blood:	n/a	n/a
20	ATF2	chrX:77150785-77151216	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chrX:77154526-77155113	GM12878	blood:	n/a	n/a
22	ATF2	chrX:77154591-77155173	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chrX:77150688-77151305	GM12878	blood:	n/a	n/a
24	ATF2	chrX:77150674-77151286	GM12878	blood:	n/a	n/a
25	ATF2	chrX:77165767-77166281	GM12878	blood:	n/a	n/a
26	ATF2	chrX:77069658-77070148	GM12878	blood:	n/a	n/a
27	ATF2	chrX:77154570-77155129	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chrX:77069630-77070170	GM12878	blood:	n/a	n/a
29	ATF2	chrX:77041510-77042003	GM12878	blood:	n/a	chrX:77041828-77041842
30	ATF3	chrX:77279939-77280189	K562	blood:	n/a	n/a
31	ATF3	chrX:77165879-77166139	H1-hESC	embryonic stem cell:	n/a	chrX:77166050-77166059 chrX:77165937-77165946
32	ATF3	chrX:77165891-77166109	K562	blood:	n/a	chrX:77166050-77166059 chrX:77165937-77165946
33	ATF3	chrX:77165856-77166146	GM12878	blood:	n/a	chrX:77166050-77166059 chrX:77165937-77165946
34	BACH1	chrX:77165858-77166178	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chrX:77301929-77302210	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chrX:77256619-77256687	K562	blood:	n/a	n/a
37	BACH1	chrX:77192784-77193063	K562	blood:	n/a	n/a
38	BCL3	chrX:77165825-77166252	GM12878	blood:	n/a	chrX:77166205-77166218 chrX:77166158-77166167 chrX:77166153-77166162 chrX:77166204-77166217 chrX:77166155-77166164 chrX:77166151-77166164 chrX:77166107-77166116 chrX:77166204-77166213
39	BCL3	chrX:77041290-77041657	A549	lung:	n/a	n/a
40	BCL3	chrX:77192816-77193220	A549	lung:	n/a	n/a
41	BCLAF1	chrX:77165787-77166156	GM12878	blood:	n/a	chrX:77166107-77166116
42	BCLAF1	chrX:77165739-77166250	GM12878	blood:	n/a	chrX:77166205-77166218 chrX:77166158-77166167 chrX:77166153-77166162 chrX:77166204-77166217 chrX:77166155-77166164 chrX:77166151-77166164 chrX:77166107-77166116 chrX:77166204-77166213
43	BCLAF1	chrX:77154513-77155026	GM12878	blood:	n/a	n/a
44	BHLHE40	chrX:77279867-77280571	HepG2	liver:	n/a	n/a
45	BHLHE40	chrX:77285470-77285487	K562	blood:	n/a	n/a
46	BHLHE40	chrX:77041450-77042009	GM12878	blood:	n/a	n/a
47	BHLHE40	chrX:77165887-77166232	A549	lung:	n/a	chrX:77166201-77166217 chrX:77166156-77166172 chrX:77166145-77166161 chrX:77166050-77166059 chrX:77166048-77166061 chrX:77166051-77166060 chrX:77165996-77166012 chrX:77166205-77166221
48	BHLHE40	chrX:77150719-77151200	GM12878	blood:	n/a	n/a
49	BHLHE40	chrX:77280257-77280584	GM12878	blood:	n/a	n/a
50	BHLHE40	chrX:77165805-77166365	HepG2	liver:	n/a	chrX:77166201-77166217 chrX:77166156-77166172 chrX:77166145-77166161 chrX:77166050-77166059 chrX:77166048-77166061 chrX:77166051-77166060 chrX:77165996-77166012 chrX:77166205-77166221

(count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:77041828-77041878	SAEC	small airway:	n/a
2	chrX:77154732-77154782	NHBE	bronchial:	n/a
3	chrX:77166237-77166287	HCM	heart:	n/a
4	chrX:77041722-77041772	SKMC	muscle:	n/a
5	chrX:77042017-77042067	HAEpiC	amniotic membrane:	n/a
6	chrX:77041828-77041878	SAEC	small airway:	n/a
7	chrX:77154732-77154782	NHBE	bronchial:	n/a
8	chrX:77166237-77166287	HCM	heart:	n/a
9	chrX:77041722-77041772	SKMC	muscle:	n/a
10	chrX:77042017-77042067	HAEpiC	amniotic membrane:	n/a
11	chrX:77154874-77154924	GM06990	blood:	n/a
12	chrX:77151237-77151287	NB4	blood:	n/a
13	chrX:77225847-77225897	BE2_C	brain:	n/a
14	chrX:77225856-77225906	AG10803	skin:	n/a
15	chrX:77041835-77041885	HepG2	liver:	n/a
16	chrX:77166237-77166287	Hepatocyte	liver:	n/a
17	chrX:77149220-77149270	Jurkat	blood:	n/a
18	chrX:77151194-77151244	CMK	blood:	n/a
19	chrX:77154821-77154871	IMR90	lung:	fetal
20	chrX:77152114-77152164	NHBE	bronchial:	n/a
21	chrX:77151065-77151115	PFSK-1	brain:	n/a
22	chrX:77041194-77041244	HPAEpiC	pulmonary alveolar:	n/a
23	chrX:77225753-77225803	HPAEpiC	pulmonary alveolar:	n/a
24	chrX:77042040-77042090	MCF10A-Er-Src	breast:	n/a
25	chrX:77147035-77147085	CMK	blood:	n/a
26	chrX:77166064-77166114	SK-N-SH_RA	brain:	n/a
27	chrX:77166064-77166114	Caco-2	colon:	n/a
28	chrX:77155144-77155194	K562	blood:	n/a
29	chrX:77041835-77041885	ProgFib	skin:	n/a
30	chrX:77041828-77041878	GM06990	blood:	n/a
31	chrX:77042539-77042589	BE2_C	brain:	n/a
32	chrX:77037960-77038010	AG04450	lung:	fetal
33	chrX:77151100-77151150	NHDF-neo	bronchial:	n/a
34	chrX:77041194-77041244	T-47D	breast:	n/a
35	chrX:77166217-77166267	HAEpiC	amniotic membrane:	n/a
36	chrX:77151042-77151092	NB4	blood:	n/a
37	chrX:77151194-77151244	GM06990	blood:	n/a
38	chrX:77084159-77084209	GM19239	blood:	n/a
39	chrX:77166064-77166114	HUVEC	blood vessel:	n/a
40	chrX:77151179-77151229	AG09309	skin:	n/a
41	chrX:77154941-77154991	SKMC	muscle:	n/a
42	chrX:77151065-77151115	SK-N-MC	brain:	n/a
43	chrX:77225138-77225188	PANC-1	pancreas:	n/a
44	chrX:77042539-77042589	HNPCEpiC	eye:	n/a
45	chrX:77166294-77166344	IMR90	lung:	fetal
46	chrX:77225138-77225188	MCF10A-Er-Src	breast:	n/a
47	chrX:77166294-77166344	HEEpiC	esophagus:	n/a
48	chrX:77154996-77155046	GM19239	blood:	n/a
49	chrX:77041194-77041244	HCF	heart:	n/a
50	chrX:77154732-77154782	PFSK-1	brain:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:77155241..77157300-chrX:77198794..77201575,2	MCF-7	breast:
2	chrX:77263570..77265987-chrX:77271725..77274130,2	K562	blood:
3	chr16:278934..279887-chrX:77040783..77041763,2	Hela-S3	cervix:
4	chrX:77153619..77156326-chrX:77166042..77168396,2	K562	blood:
5	chrX:77231965..77235028-chrX:77236693..77239954,3	K562	blood:
6	chrX:77038723..77041459-chrX:77150362..77152719,2	MCF-7	breast:
7	chrX:77171209..77173480-chrX:77175376..77179534,4	K562	blood:
8	chrX:77033474..77036528-chrX:77040329..77042995,4	MCF-7	breast:
9	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
10	chrX:77040121..77042552-chrX:77285390..77286999,2	MCF-7	breast:
11	chrX:77285841..77288705-chrX:77290926..77293069,3	MCF-7	breast:
12	chrX:75499119..75500013-chrX:77279958..77280736,2	K562	blood:
13	chrX:77156256..77158381-chrX:77359594..77361114,2	MCF-7	breast:
14	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
15	chrX:77149002..77152888-chrX:77153078..77156391,9	MCF-7	breast:
16	chrX:77183775..77185669-chrX:77187264..77189989,2	K562	blood:
17	chr15:90931452..90932078-chrX:77041481..77042209,2	Hela-S3	cervix:
18	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
19	chrX:77155011..77157047-chrX:77164638..77166954,2	MCF-7	breast:
20	chrX:76996384..76998942-chrX:77041132..77042972,2	MCF-7	breast:
21	chrX:77285841..77288705-chrX:77290926..77293069,3	MCF-7	breast:
22	chrX:77198884..77200659-chrX:77206584..77208164,2	K562	blood:
23	chrX:77155241..77157300-chrX:77198794..77201575,2	MCF-7	breast:
24	chr15:41575813..41576546-chrX:77150464..77151239,2	Hela-S3	cervix:
25	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
26	chrX:77034724..77036644-chrX:77040474..77043894,3	K562	blood:
27	chr19:38269810..38270643-chrX:77154544..77155428,2	Hela-S3	cervix:
28	chrX:77199002..77201329-chrX:77206081..77208457,2	K562	blood:
29	chrX:76993528..76995377-chrX:76996626..76999172,2	MCF-7	breast:
30	chrX:77164605..77167302-chrX:77357779..77361008,3	K562	blood:
31	chrX:77228292..77229799-chrX:77231409..77232965,2	MCF-7	breast:
32	chrX:77231965..77235028-chrX:77236693..77239954,3	K562	blood:
33	chrX:77142206..77144485-chrX:77148518..77150747,2	K562	blood:
34	chrX:77300334..77302047-chrX:77359005..77361971,2	K562	blood:
35	chrX:77183775..77185669-chrX:77187264..77189989,2	K562	blood:
36	chrX:77171209..77173480-chrX:77175376..77179534,4	K562	blood:
37	chrX:77231280..77233851-chrX:77237053..77239063,3	K562	blood:
38	chrX:77262120..77263891-chrX:77267020..77269535,2	K562	blood:
39	chrX:77154406..77156573-chrX:77174555..77176818,2	K562	blood:
40	chrX:77153329..77155413-chrX:77248472..77249987,2	K562	blood:
41	chrX:77040998..77042941-chrX:77180731..77182712,2	K562	blood:
42	chrX:77153159..77156073-chrX:77281305..77283544,2	MCF-7	breast:
43	chrX:77147137..77148807-chrX:77150404..77151960,2	K562	blood:
44	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
45	chrX:77164918..77166473-chrX:77167959..77169910,2	K562	blood:
46	chrX:77147137..77149417-chrX:77149428..77151904,2	K562	blood:
47	chrX:77164674..77168501-chrX:77176540..77178138,3	K562	blood:
48	chrX:77038824..77040402-chrX:77040852..77043710,2	MCF-7	breast:
49	chr19:2475673..2476376-chrX:77150560..77151320,2	Hela-S3	cervix:
50	chrX:76927164..76929589-chrX:77151949..77154755,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX7B-3	chrX:77140874-77141127	NONHSAT137693
2	lnc-COX7B-1	chrX:77158140-77158693	NONHSAT137695
3	lnc-PGK1-3	chrX:77261614-77261936	expReg_chrX_4933_+
4	lnc-PGK1-2	chrX:77263703-77263995	expReg_chrX_4934_+
5	lnc-COX7B-1	chrX:77154960-77155090	NONHSAT137695
6	lnc-COX7B-4	chrX:77166238-77166332	NONHSAT137698
7	lnc-COX7B-4	chrX:77218120-77220387	NONHSAT137698
8	lnc-COX7B-2	chrX:77162205-77163540	NONHSAT137697
9	lnc-COX7B-5	chrX:76983344-76983557	NONHSAT137691

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PGAM4	hsa-miR-92b-3p	chrX:77223458-77223479
2	ATP7A	hsa-miR-148b-3p	chrX:77302103-77302110
3	COX7B	hsa-miR-17-5p	chrX:77160805-77160829
4	ATP7A	hsa-miR-320a	chrX:77302588-77302611
5	MAGT1	hsa-miR-124-3p	chrX:77084555-77084574
6	ATP7A	hsa-miR-148b-3p	chrX:77302089-77302110
7	MAGT1	hsa-miR-124-3p	chrX:77082022-77082015
8	ATP7A	hsa-miR-9-5p	chrX:77304997-77305003
9	MAGT1	hsa-miR-124-3p	chrX:77082016-77082037
10	PGAM4	hsa-miR-181d-5p	chrX:77223917-77223937
11	MAGT1	hsa-miR-124-3p	chrX:77084561-77084554

Variant related genes	Relation type
COX7B	TF binding region
ATRX	TF binding region
PGAM4	TF binding region
FABP5P15	TF binding region
MAGT1	TF binding region
ENSG00000248503	TF binding region
ATP7A	TF binding region
RNU6-854P	TF binding region
RN7SL460P	TF binding region
COX7B	CpG island
ATRX	CpG island
PGAM4	CpG island
FABP5P15	CpG island
MAGT1	CpG island
ENSG00000248503	CpG island
ATP7A	CpG island
RNU6-854P	CpG island
RN7SL460P	CpG island
ENSG00000140575	chromatin interactions
ENSG00000085224	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000178252	chromatin interactions
ENSG00000165240	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000248503	chromatin interactions
ENSG00000102144	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000108840	chromatin interactions
ENSG00000111640	chromatin interactions
ENSG00000131174	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000267422	chromatin interactions
ENSG00000189144	chromatin interactions
ENSG00000247556	chromatin interactions
ENSG00000007392	chromatin interactions
ENSG00000102158	chromatin interactions

Extended variants
information (count: 3673 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:3673 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185982350	chrX:76969069-76969070	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs12394882	chrX:76969205-76969206	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs138458513	chrX:76969244-76969245	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs45604641	chrX:76969292-76969293	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs143095115	chrX:76969375-76969376	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs576550941	chrX:76969452-76969453	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs191531819	chrX:76969488-76969489	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs181245964	chrX:76969509-76969510	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs7884553	chrX:76969685-76969686	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs186276350	chrX:76969807-76969808	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs373771607	chrX:76969834-76969835	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs190798651	chrX:76969848-76969849	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs182078970	chrX:76970005-76970006	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs187824260	chrX:76970018-76970019	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs34523053	chrX:76970232-76970233	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs35874589	chrX:76970250-76970251	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs45552532	chrX:76970354-76970355	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs190793701	chrX:76970358-76970359	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs555823919	chrX:76970406-76970407	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs45579339	chrX:76970417-76970418	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs45503491	chrX:76970511-76970512	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs182990484	chrX:76970670-76970671	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs45625240	chrX:76970844-76970845	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs187306440	chrX:76970863-76970864	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs192987388	chrX:76970875-76970876	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs541454547	chrX:76971120-76971121	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs532012142	chrX:76971241-76971242	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs184740969	chrX:76971285-76971286	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs188067913	chrX:76971290-76971291	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs145202341	chrX:76971402-76971403	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs199639051	chrX:76971602-76971603	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs192354869	chrX:76971618-76971619	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs183658271	chrX:76971727-76971728	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs189549915	chrX:76971987-76971988	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs192447391	chrX:76972088-76972089	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184693364	chrX:76972209-76972210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189974840	chrX:76972266-76972267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550519756	chrX:76972366-76972367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181616375	chrX:76972574-76972575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201926888	chrX:76972585-76972586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149990714	chrX:76972623-76972624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201353033	chrX:76972627-76972628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs122445108	chrX:76972632-76972633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199948087	chrX:76972645-76972646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202181116	chrX:76972741-76972742	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs367730391	chrX:76972751-76972752	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs200930277	chrX:76972763-76972764	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186384799	chrX:76972784-76972785	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs140590017	chrX:76972821-76972822	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs189717179	chrX:76972905-76972906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
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
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
Alcoholism	21790672	CNVD
Mental retardation	22129561	CNVD
small cell lung cancer	20016488	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD

Chromatin state (count:3981 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76860400-76974400	Weak transcription	HepG2	liver
2	chrX:76873000-76979400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chrX:76895800-76970600	Weak transcription	Stomach Smooth Muscle	stomach
4	chrX:76896400-76969400	Weak transcription	Primary T cells from cord blood	blood
5	chrX:76907800-76975000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chrX:76925000-76972800	Weak transcription	Pancreas	Pancrea
7	chrX:76928000-76970600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chrX:76929400-76973600	Weak transcription	NHLF	lung
9	chrX:76931000-76972000	Weak transcription	Aorta	Aorta
10	chrX:76938000-76974600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chrX:76944400-76969200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chrX:76944800-76973200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chrX:76946400-76973000	Weak transcription	Fetal Kidney	kidney
14	chrX:76947800-76972000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chrX:76947800-76974200	Weak transcription	H1 Cell Line	embryonic stem cell
16	chrX:76948400-76971000	Weak transcription	Fetal Heart	heart
17	chrX:76948800-76976400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chrX:76950200-76973000	Weak transcription	Brain Anterior Caudate	brain
19	chrX:76950800-76975200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chrX:76952200-76969600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chrX:76952600-76971200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chrX:76952600-76973000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chrX:76953600-76969200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chrX:76953800-76972400	Weak transcription	NH-A	brain
25	chrX:76954000-76970400	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chrX:76954000-76974200	Weak transcription	A549	lung
27	chrX:76954400-76970600	Weak transcription	HSMM	muscle
28	chrX:76955800-76970600	Weak transcription	Colon Smooth Muscle	Colon
29	chrX:76957400-76973600	Weak transcription	Spleen	Spleen
30	chrX:76959000-76972000	Weak transcription	Ovary	ovary
31	chrX:76959600-76969200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chrX:76959800-76973800	Weak transcription	Primary hematopoietic stem cells	blood
33	chrX:76960000-76969400	Weak transcription	Duodenum Mucosa	Duodenum
34	chrX:76960000-76971400	Weak transcription	Fetal Brain Female	brain
35	chrX:76960200-76969200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chrX:76960200-76971400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chrX:76960200-76973000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chrX:76960200-76974400	Weak transcription	Primary B cells from cord blood	blood
39	chrX:76960600-76973400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chrX:76960600-76974200	Weak transcription	Brain Germinal Matrix	brain
41	chrX:76960800-76972400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chrX:76960800-76973200	Weak transcription	Gastric	stomach
43	chrX:76960800-76979400	Weak transcription	Psoas Muscle	Psoas
44	chrX:76961000-76969200	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chrX:76961000-76970400	Weak transcription	Fetal Thymus	thymus
46	chrX:76961000-76971600	Weak transcription	Fetal Muscle Leg	muscle
47	chrX:76961000-76972400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chrX:76961000-76972800	Weak transcription	Left Ventricle	heart
49	chrX:76961000-76973600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chrX:76961000-76973600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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