Variant report

Variant	esv2758569
Chromosome Location	chrX:56739069-56887748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3018)
CpG islands
(count:367)
Chromatin interactive
region (count:39)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:56752993-56753362	K562	blood:	n/a	n/a
2	ATF2	chrX:56790124-56790541	GM12878	blood:	n/a	n/a
3	ATF2	chrX:56790827-56791243	GM12878	blood:	n/a	n/a
4	ATF2	chrX:56790757-56791316	GM12878	blood:	n/a	n/a
5	ATF3	chrX:56771415-56771798	HCT-116	colon:	n/a	n/a
6	ATF3	chrX:56771375-56771803	HCT-116	colon:	n/a	n/a
7	BACH1	chrX:56846929-56847120	K562	blood:	n/a	n/a
8	BACH1	chrX:56861087-56861214	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chrX:56794004-56794474	GM12878	blood:	n/a	n/a
10	BATF	chrX:56804693-56805278	GM12878	blood:	n/a	n/a
11	BATF	chrX:56794060-56794375	GM12878	blood:	n/a	n/a
12	BATF	chrX:56799455-56799777	GM12878	blood:	n/a	n/a
13	BATF	chrX:56800171-56800397	GM12878	blood:	n/a	n/a
14	BATF	chrX:56804857-56805179	GM12878	blood:	n/a	n/a
15	BATF	chrX:56805573-56805799	GM12878	blood:	n/a	n/a
16	BATF	chrX:56799291-56799876	GM12878	blood:	n/a	n/a
17	BATF	chrX:56852491-56852714	GM12878	blood:	n/a	n/a
18	BATF	chrX:56794769-56794995	GM12878	blood:	n/a	n/a
19	BATF	chrX:56788750-56789058	GM12878	blood:	n/a	n/a
20	BATF	chrX:56839721-56840063	GM12878	blood:	n/a	n/a
21	BATF	chrX:56805283-56805958	GM12878	blood:	n/a	n/a
22	BATF	chrX:56843625-56843859	GM12878	blood:	n/a	n/a
23	BATF	chrX:56794479-56795154	GM12878	blood:	n/a	n/a
24	BATF	chrX:56799881-56800556	GM12878	blood:	n/a	n/a
25	BCL11A	chrX:56799865-56800568	GM12878	blood:	n/a	chrX:56800208-56800217 chrX:56800067-56800080
26	BCL11A	chrX:56799432-56799693	GM12878	blood:	n/a	n/a
27	BCL11A	chrX:56794463-56795166	GM12878	blood:	n/a	chrX:56794806-56794815 chrX:56794665-56794678
28	BCL11A	chrX:56805267-56805970	GM12878	blood:	n/a	chrX:56805469-56805482 chrX:56805610-56805619
29	BCL11A	chrX:56804834-56805095	GM12878	blood:	n/a	n/a
30	BCL11A	chrX:56799196-56800628	GM12878	blood:	n/a	chrX:56800208-56800217 chrX:56800067-56800080 chrX:56799267-56799280
31	BCL11A	chrX:56794063-56794291	GM12878	blood:	n/a	n/a
32	BCL11A	chrX:56804598-56806030	GM12878	blood:	n/a	chrX:56804669-56804682 chrX:56805469-56805482 chrX:56805610-56805619
33	BCL11A	chrX:56793982-56795226	GM12878	blood:	n/a	chrX:56794806-56794815 chrX:56794665-56794678
34	BCLAF1	chrX:56790707-56791389	GM12878	blood:	n/a	chrX:56790930-56790939 chrX:56790789-56790802
35	BCLAF1	chrX:56809838-56810400	GM12878	blood:	n/a	chrX:56810049-56810058
36	BCLAF1	chrX:56759936-56760248	GM12878	blood:	n/a	n/a
37	BCLAF1	chrX:56829707-56830407	GM12878	blood:	n/a	chrX:56829754-56829762
38	BCLAF1	chrX:56753084-56753420	GM12878	blood:	n/a	n/a
39	BCLAF1	chrX:56809929-56810339	GM12878	blood:	n/a	chrX:56810049-56810058
40	BCLAF1	chrX:56790075-56791158	GM12878	blood:	n/a	chrX:56790419-56790428 chrX:56790418-56790427 chrX:56790930-56790939 chrX:56790789-56790802
41	BCLAF1	chrX:56790121-56790609	GM12878	blood:	n/a	chrX:56790419-56790428 chrX:56790418-56790427
42	BCLAF1	chrX:56829256-56829591	GM12878	blood:	n/a	n/a
43	BCLAF1	chrX:56829943-56830357	GM12878	blood:	n/a	n/a
44	BHLHE40	chrX:56788686-56792802	GM12878	blood:	n/a	n/a
45	BHLHE40	chrX:56839778-56840206	K562	blood:	n/a	n/a
46	BHLHE40	chrX:56839368-56839385	GM12878	blood:	n/a	n/a
47	BHLHE40	chrX:56839630-56840074	GM12878	blood:	n/a	n/a
48	BHLHE40	chrX:56755682-56755909	GM12878	blood:	n/a	n/a
49	BHLHE40	chrX:56871346-56871448	K562	blood:	n/a	n/a
50	BHLHE40	chrX:56829928-56830314	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:56756686-56756736	SK-N-MC	brain:	n/a
2	chrX:56756686-56756736	SK-N-MC	brain:	n/a
3	chrX:56756686-56756736	NB4	blood:	n/a
4	chrX:56756686-56756736	Jurkat	blood:	n/a
5	chrX:56756686-56756736	AG09319	gingival:	n/a
6	chrX:56755717-56755767	SK-N-MC	brain:	n/a
7	chrX:56755717-56755767	NT2-D1	testis:	n/a
8	chrX:56755714-56755764	SKMC	muscle:	n/a
9	chrX:56764293-56764343	AG10803	skin:	n/a
10	chrX:56755714-56755764	BJ	skin:	n/a
11	chrX:56755717-56755767	NB4	blood:	n/a
12	chrX:56764796-56764846	U87	brain:	n/a
13	chrX:56755717-56755767	HEK293	kidney:	embryo
14	chrX:56764293-56764343	AG09319	gingival:	n/a
15	chrX:56755717-56755767	K562	blood:	n/a
16	chrX:56755717-56755767	ProgFib	skin:	n/a
17	chrX:56755717-56755767	BE2_C	brain:	n/a
18	chrX:56754534-56754584	AG09309	skin:	n/a
19	chrX:56756686-56756736	HEEpiC	esophagus:	n/a
20	chrX:56764796-56764846	HAEpiC	amniotic membrane:	n/a
21	chrX:56764293-56764343	K562	blood:	n/a
22	chrX:56764293-56764343	RPTEC	kidney:	n/a
23	chrX:56754534-56754584	PANC-1	pancreas:	n/a
24	chrX:56756686-56756736	SKMC	muscle:	n/a
25	chrX:56764293-56764343	BE2_C	brain:	n/a
26	chrX:56756686-56756736	NHBE	bronchial:	n/a
27	chrX:56764796-56764846	NB4	blood:	n/a
28	chrX:56756686-56756736	HCF	heart:	n/a
29	chrX:56755714-56755764	RPTEC	kidney:	n/a
30	chrX:56755714-56755764	SK-N-SH_RA	brain:	n/a
31	chrX:56754534-56754584	MCF10A-Er-Src	breast:	n/a
32	chrX:56754534-56754584	MCF-7	breast:	n/a
33	chrX:56764796-56764846	SK-N-MC	brain:	n/a
34	chrX:56756686-56756736	HAEpiC	amniotic membrane:	n/a
35	chrX:56764796-56764846	IMR90	lung:	fetal
36	chrX:56756686-56756736	ECC-1	luminal epithelium:	n/a
37	chrX:56755717-56755767	HRE	kidney:	n/a
38	chrX:56764293-56764343	HL-60	blood:	n/a
39	chrX:56764796-56764846	HCF	heart:	n/a
40	chrX:56764796-56764846	GM19239	blood:	n/a
41	chrX:56755717-56755767	AoSMC	blood vessel:	n/a
42	chrX:56764796-56764846	CMK	blood:	n/a
43	chrX:56755714-56755764	HCM	heart:	n/a
44	chrX:56755717-56755767	AG09309	skin:	n/a
45	chrX:56764293-56764343	CMK	blood:	n/a
46	chrX:56755714-56755764	HAEpiC	amniotic membrane:	n/a
47	chrX:56764293-56764343	Caco-2	colon:	n/a
48	chrX:56764796-56764846	RPTEC	kidney:	n/a
49	chrX:56756686-56756736	PFSK-1	brain:	n/a
50	chrX:56756686-56756736	AoSMC	blood vessel:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:56806832..56808536-chrX:56810379..56813330,2	MCF-7	breast:
2	chrX:56814414..56817142-chrX:56827213..56829946,2	MCF-7	breast:
3	chrX:56830015..56830949-chrX:57004313..57005248,9	MCF-7	breast:
4	chrX:56589521..56592004-chrX:56754888..56757482,3	MCF-7	breast:
5	chrX:56820104..56822444-chrX:56825427..56828204,2	MCF-7	breast:
6	chrX:56815404..56816431-chrX:57001867..57002525,3	MCF-7	breast:
7	chrX:56816463..56818432-chrX:56827430..56829351,2	MCF-7	breast:
8	chrX:56816463..56818432-chrX:56827430..56829351,2	MCF-7	breast:
9	chrX:56755952..56758658-chrX:56787740..56790221,2	MCF-7	breast:
10	chrX:56884085..56885969-chrX:56889325..56892180,2	MCF-7	breast:
11	chrX:56820104..56822444-chrX:56825427..56828204,2	MCF-7	breast:
12	chrX:56839314..56842023-chrX:57019639..57021323,2	MCF-7	breast:
13	chrX:56784028..56786662-chrX:56837898..56840696,2	MCF-7	breast:
14	chrX:56755952..56758658-chrX:56787740..56790221,2	MCF-7	breast:
15	chrX:56790542..56791292-chrX:57182607..57183519,2	MCF-7	breast:
16	chrX:56790522..56791427-chrX:57004320..57005681,3	MCF-7	breast:
17	chrX:56830136..56831999-chrX:57005582..57007963,2	MCF-7	breast:
18	chrX:56815042..56815706-chrX:57004646..57005228,2	MCF-7	breast:
19	chrX:56790745..56791532-chrX:57002195..57003144,2	K562	blood:
20	chrX:56488558..56489404-chrX:56753028..56753703,4	MCF-7	breast:
21	chrX:56839755..56841638-chrX:56845784..56848486,2	K562	blood:
22	chrX:56816736..56818611-chrX:56825316..56827137,2	MCF-7	breast:
23	chrX:56814414..56817142-chrX:56827213..56829946,2	MCF-7	breast:
24	chrX:56820591..56822827-chrX:56824334..56826679,2	MCF-7	breast:
25	chrX:56790021..56792634-chrX:56811164..56813731,2	MCF-7	breast:
26	chrX:56806832..56808536-chrX:56810379..56813330,2	MCF-7	breast:
27	chrX:56839755..56841638-chrX:56845784..56848486,2	K562	blood:
28	chrX:56850607..56853538-chrX:57149099..57151794,2	K562	blood:
29	chrX:56308361..56308892-chrX:56752872..56753378,2	K562	blood:
30	chrX:56809606..56814418-chrX:56815131..56818953,4	MCF-7	breast:
31	chrX:56816736..56818611-chrX:56825316..56827137,2	MCF-7	breast:
32	chrX:56784028..56786662-chrX:56837898..56840696,2	MCF-7	breast:
33	chrX:56820591..56822827-chrX:56824334..56826679,2	MCF-7	breast:
34	chrX:56754417..56757216-chrX:56757629..56759617,2	MCF-7	breast:
35	chrX:56790021..56792634-chrX:56811164..56813731,2	MCF-7	breast:
36	chr17:41466274..41467888-chrX:56858614..56860134,2	K562	blood:
37	chrX:56809606..56814418-chrX:56815131..56818953,4	MCF-7	breast:
38	chrX:56815042..56815858-chrX:57555231..57555778,2	MCF-7	breast:
39	chrX:56829971..56830601-chrX:57001746..57002383,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPIN3-3	chrX:56778876-56779216	NONHSAT137276
2	lnc-UBQLN2-5	chrX:56760584-56761001	NONHSAT137274
3	lnc-SPIN3-2	chrX:56815479-56815983	NONHSAT137277
4	lnc-SPIN3-3	chrX:56790854-56790965	NONHSAT137276
5	lnc-UBQLN2-7	chrX:56772443-56772747	ucscGeneNc_uc004dut_2
6	lnc-SPIN3-2	chrX:56808673-56808686	NONHSAT137277
7	lnc-SPIN3-3	chrX:56789313-56789333	NONHSAT137276
8	lnc-SPIN3-2	chrX:56808145-56808617	NONHSAT137277
9	lnc-SPIN3-2	chrX:56823800-56824231	NONHSAT137277
10	lnc-UBQLN2-7	chrX:56775221-56775357	ucscGeneNc_uc004dut_2
11	lnc-UBQLN2-4	chrX:56759851-56760504	NONHSAT137273
12	lnc-UBQLN2-7	chrX:56860478-56860729	ucscGeneNc_uc004dut_2
13	lnc-SPIN3-3	chrX:56788470-56788737	NONHSAT137276
14	lnc-SPIN3-2	chrX:56825775-56826193	NONHSAT137277
15	lnc-SPIN3-2	chrX:56826891-56827336	NONHSAT137277
16	lnc-UBQLN2-6	chrX:56762139-56762989	NONHSAT137275
17	lnc-SPIN3-4	chrX:56763221-56764017	NR_002308

No data

Variant related genes	Relation type
UQCRBP1	TF binding region
ENSG00000204272	TF binding region
UQCRBP1	CpG island
ENSG00000204272	CpG island
ENSG00000188021	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 1457 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:1457 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61429868	chrX:56750969-56750970	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150779923	chrX:56750974-56750975	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs191747138	chrX:56751000-56751001	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368322159	chrX:56751007-56751008	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs183175370	chrX:56752705-56752706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs57180538	chrX:56752847-56752848	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs7876419	chrX:56752855-56752856	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs78524489	chrX:56752921-56752922	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201972787	chrX:56753038-56753039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111760660	chrX:56753040-56753041	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs66764349	chrX:56753041-56753042	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs141724485	chrX:56753044-56753045	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs187505494	chrX:56753070-56753071	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs73626217	chrX:56753077-56753078	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs147906437	chrX:56753106-56753107	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141537253	chrX:56753115-56753116	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373284782	chrX:56753141-56753142	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191866439	chrX:56753176-56753177	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs5914776	chrX:56753179-56753180	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182613399	chrX:56753188-56753189	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572101456	chrX:56753275-56753276	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs73494903	chrX:56753293-56753294	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545967119	chrX:56753538-56753539	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs374974302	chrX:56753604-56753605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187957330	chrX:56753661-56753662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564171390	chrX:56753783-56753784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17277469	chrX:56753784-56753785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192151515	chrX:56753798-56753799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143605630	chrX:56753856-56753857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372677457	chrX:56753948-56753949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs5960785	chrX:56753997-56753998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185725042	chrX:56754109-56754110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190550014	chrX:56754138-56754139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142579642	chrX:56754139-56754140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565966598	chrX:56754186-56754187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144659575	chrX:56754271-56754272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192490851	chrX:56754375-56754376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184442527	chrX:56754377-56754378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188888870	chrX:56754406-56754407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181257236	chrX:56754566-56754567	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs199885292	chrX:56754567-56754568	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs138611323	chrX:56754761-56754762	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs1927223	chrX:56754961-56754962	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs1927222	chrX:56755018-56755019	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs374813021	chrX:56755056-56755057	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1927221	chrX:56755141-56755142	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs78522345	chrX:56755160-56755161	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570337382	chrX:56755216-56755217	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185346816	chrX:56755340-56755341	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs139044633	chrX:56755378-56755379	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Cancer	16751803	CNVD
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	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
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Thyroid cancer	19087340	CNVD
lymphocytic leukemia	21291569	CNVD
Cervical cancer	21062161	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2740 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:56752800-56755200	Enhancers	Liver	Liver
2	chrX:56753200-56753400	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chrX:56753200-56753400	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chrX:56753200-56753600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chrX:56753200-56754600	Enhancers	Dnd41	blood
6	chrX:56753400-56754400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chrX:56753400-56754800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chrX:56753600-56755000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chrX:56754000-56755200	Enhancers	Brain Hippocampus Middle	brain
10	chrX:56754400-56754600	Enhancers	Brain Substantia Nigra	brain
11	chrX:56754400-56755000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chrX:56754400-56755200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chrX:56754600-56754800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chrX:56754600-56754800	Bivalent Enhancer	Fetal Brain Male	brain
15	chrX:56754600-56755000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chrX:56754600-56755000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chrX:56754600-56755400	Flanking Active TSS	Dnd41	blood
18	chrX:56754600-56755600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chrX:56754600-56757600	Active TSS	A549	lung
20	chrX:56754600-56757800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chrX:56754800-56755000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chrX:56754800-56755000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chrX:56754800-56755000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chrX:56754800-56755000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chrX:56754800-56755000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chrX:56754800-56755000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chrX:56754800-56755200	Enhancers	H1 Cell Line	embryonic stem cell
28	chrX:56754800-56755200	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chrX:56754800-56755200	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chrX:56754800-56755200	Enhancers	Fetal Intestine Small	intestine
31	chrX:56754800-56755200	Bivalent Enhancer	Fetal Kidney	kidney
32	chrX:56754800-56755200	Enhancers	Hela-S3	cervix
33	chrX:56754800-56755600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chrX:56754800-56757200	Active TSS	Muscle Satellite Cultured Cells	--
35	chrX:56754800-56757200	Active TSS	Brain Angular Gyrus	brain
36	chrX:56754800-56757200	Active TSS	NHDF-Ad	bronchial
37	chrX:56754800-56757400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chrX:56754800-56757400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chrX:56754800-56757400	Active TSS	NH-A	brain
40	chrX:56754800-56757600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chrX:56754800-56757600	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chrX:56754800-56758600	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chrX:56755000-56755200	Enhancers	Primary B cells from cord blood	blood
44	chrX:56755000-56755200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chrX:56755000-56755200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chrX:56755000-56755200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chrX:56755000-56755200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chrX:56755000-56755200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chrX:56755000-56755800	Active TSS	Cortex derived primary cultured neurospheres	brain
50	chrX:56755000-56755800	Active TSS	Osteobl	bone

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