Variant report

Variant	nsv529913
Chromosome Location	chrX:78605903-79090819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1493)
CpG islands
(count:428)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1493 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:78619848-78620082	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:78705812-78706026	K562	blood:	n/a	n/a
3	ARID3A	chrX:78705834-78706050	HepG2	liver:	n/a	n/a
4	BACH1	chrX:78622927-78623123	K562	blood:	n/a	n/a
5	BATF	chrX:78735482-78735650	GM12878	blood:	n/a	n/a
6	BATF	chrX:78885743-78886112	GM12878	blood:	n/a	n/a
7	BATF	chrX:78885772-78886094	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:78887341-78887467	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:78623624-78623797	GM12878	blood:	n/a	n/a
10	BHLHE40	chrX:78705870-78705988	GM12878	blood:	n/a	n/a
11	BHLHE40	chrX:78622320-78623349	K562	blood:	n/a	n/a
12	BHLHE40	chrX:78622383-78623243	GM12878	blood:	n/a	n/a
13	BRCA1	chrX:79039053-79039097	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chrX:78902429-78902462	GM12878	blood:	n/a	n/a
15	CBX3	chrX:78679851-78680040	K562	blood:	n/a	n/a
16	CBX3	chrX:78679880-78680065	K562	blood:	n/a	n/a
17	CBX3	chrX:78622932-78623236	K562	blood:	n/a	n/a
18	CCNT2	chrX:78622220-78623187	K562	blood:	n/a	chrX:78622571-78622580
19	CEBPB	chrX:78787419-78787664	MCF-7	breast:	n/a	chrX:78787584-78787595
20	CEBPB	chrX:78954411-78954618	IMR90	lung:	n/a	n/a
21	CEBPB	chrX:79020611-79020784	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:78921262-78921462	IMR90	lung:	n/a	n/a
23	CEBPB	chrX:78888884-78889153	HepG2	liver:	n/a	chrX:78889057-78889068 chrX:78889043-78889054
24	CEBPB	chrX:78888919-78889149	A549	lung:	n/a	chrX:78889057-78889068 chrX:78889043-78889054
25	CEBPB	chrX:79053438-79053631	A549	lung:	n/a	n/a
26	CEBPB	chrX:78899082-78899357	IMR90	lung:	n/a	n/a
27	CEBPB	chrX:78619864-78620174	HepG2	liver:	n/a	n/a
28	CEBPB	chrX:78787499-78787686	H1-hESC	embryonic stem cell:	n/a	chrX:78787584-78787595
29	CEBPB	chrX:79053401-79053570	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chrX:78846653-78846908	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:78622947-78623197	K562	blood:	n/a	n/a
32	CEBPB	chrX:78787444-78787721	HepG2	liver:	n/a	chrX:78787584-78787595
33	CEBPB	chrX:78619906-78620219	K562	blood:	n/a	n/a
34	CEBPB	chrX:78904275-78904480	HepG2	liver:	n/a	chrX:78904306-78904317
35	CEBPB	chrX:78902917-78903215	HepG2	liver:	n/a	chrX:78903096-78903107
36	CEBPB	chrX:78787453-78787776	IMR90	lung:	n/a	chrX:78787584-78787595
37	CEBPB	chrX:78902961-78903255	IMR90	lung:	n/a	chrX:78903096-78903107
38	CEBPB	chrX:78611876-78612152	K562	blood:	n/a	n/a
39	CEBPB	chrX:78675590-78675847	K562	blood:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
40	CEBPB	chrX:79053414-79053622	MCF-7	breast:	n/a	n/a
41	CEBPB	chrX:78918014-78918214	HepG2	liver:	n/a	chrX:78918126-78918137 chrX:78918104-78918115
42	CEBPB	chrX:78781572-78781859	HepG2	liver:	n/a	chrX:78781690-78781701
43	CEBPB	chrX:78622768-78623232	K562	blood:	n/a	n/a
44	CEBPB	chrX:79053317-79053696	IMR90	lung:	n/a	n/a
45	CEBPB	chrX:79053400-79053674	K562	blood:	n/a	n/a
46	CEBPB	chrX:78787431-78787758	A549	lung:	n/a	chrX:78787584-78787595
47	CEBPB	chrX:78904168-78904463	IMR90	lung:	n/a	chrX:78904306-78904317
48	CEBPB	chrX:78675506-78675787	HepG2	liver:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
49	CEBPB	chrX:78675550-78675840	IMR90	lung:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
50	CEBPB	chrX:78877237-78877446	HepG2	liver:	n/a	chrX:78877347-78877358

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:78623745-78623795	PFSK-1	brain:	n/a
2	chrX:78623745-78623795	PFSK-1	brain:	n/a
3	chrX:78623745-78623795	Caco-2	colon:	n/a
4	chrX:78623956-78624006	HepG2	liver:	n/a
5	chrX:78623745-78623795	MCF10A-Er-Src	breast:	n/a
6	chrX:78622859-78622909	AG10803	skin:	n/a
7	chrX:78623020-78623070	GM12891	blood:	n/a
8	chrX:78623020-78623070	NT2-D1	testis:	n/a
9	chrX:78623745-78623795	AG09309	skin:	n/a
10	chrX:78622565-78622615	HIPEpiC	eye:	n/a
11	chrX:78622682-78622732	HCF	heart:	n/a
12	chrX:78623745-78623795	HMEC	breast:	n/a
13	chrX:78622859-78622909	HCF	heart:	n/a
14	chrX:78622859-78622909	NHDF-neo	bronchial:	n/a
15	chrX:78622859-78622909	PrEC	prostate:	n/a
16	chrX:78622682-78622732	A549	lung:	n/a
17	chrX:78624108-78624158	Jurkat	blood:	n/a
18	chrX:78623745-78623795	HCF	heart:	n/a
19	chrX:78622859-78622909	HRCEpiC	kidney:	n/a
20	chrX:78623745-78623795	GM12891	blood:	n/a
21	chrX:78624108-78624158	SK-N-SH	brain:	n/a
22	chrX:78622859-78622909	HEK293	kidney:	embryo
23	chrX:78624108-78624158	CMK	blood:	n/a
24	chrX:78623745-78623795	HRPEpiC	eye:	n/a
25	chrX:78622682-78622732	AG09309	skin:	n/a
26	chrX:78622565-78622615	HUVEC	blood vessel:	n/a
27	chrX:78622565-78622615	RPTEC	kidney:	n/a
28	chrX:78622565-78622615	H1-hESC	embryonic stem cell:	embryo
29	chrX:78622565-78622615	MCF-7	breast:	n/a
30	chrX:78622682-78622732	H1-hESC	embryonic stem cell:	embryo
31	chrX:78622682-78622732	SAEC	small airway:	n/a
32	chrX:78624108-78624158	H1-hESC	embryonic stem cell:	embryo
33	chrX:78622859-78622909	T-47D	breast:	n/a
34	chrX:78623956-78624006	AG10803	skin:	n/a
35	chrX:78623020-78623070	AG10803	skin:	n/a
36	chrX:78623020-78623070	HIPEpiC	eye:	n/a
37	chrX:78622682-78622732	NHDF-neo	bronchial:	n/a
38	chrX:78622565-78622615	NHDF-neo	bronchial:	n/a
39	chrX:78623745-78623795	Hepatocyte	liver:	n/a
40	chrX:78622565-78622615	IMR90	lung:	fetal
41	chrX:78624108-78624158	ECC-1	luminal epithelium:	n/a
42	chrX:78623745-78623795	HIPEpiC	eye:	n/a
43	chrX:78624108-78624158	MCF10A-Er-Src	breast:	n/a
44	chrX:78622859-78622909	SK-N-SH_RA	brain:	n/a
45	chrX:78623956-78624006	HCM	heart:	n/a
46	chrX:78622859-78622909	PFSK-1	brain:	n/a
47	chrX:78623956-78624006	SKMC	muscle:	n/a
48	chrX:78622682-78622732	LNCaP	prostate:	n/a
49	chrX:78622859-78622909	HCT-116	colon:	n/a
50	chrX:78623956-78624006	HL-60	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:78733188..78733978-chrX:79285640..79286468,2	MCF-7	breast:
2	chrX:78612180..78614323-chrX:78618566..78621520,2	K562	blood:
3	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
4	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
5	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
6	chr2:219180197..219181031-chrX:78672273..78672996,2	HCT-116	colon:
7	chrX:78615804..78618128-chrX:78622582..78624536,2	K562	blood:
8	chrX:78600900..78603777-chrX:78604763..78607370,2	MCF-7	breast:
9	chrX:77810661..77811278-chrX:78780189..78780762,2	MCF-7	breast:
10	chr8:110352840..110355386-chrX:78849788..78852363,2	MCF-7	breast:
11	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
12	chrX:77811500..77813088-chrX:78666250..78667785,2	MCF-7	breast:
13	chr8:55770247..55770767-chrX:78893853..78894478,2	MCF-7	breast:
14	chrX:78613371..78615323-chrX:78622479..78624740,2	K562	blood:
15	chr9:119319099..119319741-chrX:79019251..79019874,2	MCF-7	breast:
16	chrX:78611688..78613722-chrX:78621637..78623492,2	K562	blood:
17	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
18	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
19	chr15:79105202..79107134-chrX:78755858..78757584,2	MCF-7	breast:
20	chrX:78623909..78625908-chrX:78627039..78629119,3	K562	blood:
21	chr11:118881446..118882428-chrX:78719744..78720315,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITM2A-2	chrX:78624861-78625662	NONHSAT137716

No data

Variant related genes	Relation type
ENSG00000270268	TF binding region
ITM2A	TF binding region
ENSG00000270268	CpG island
ITM2A	CpG island
ENSG00000186166	chromatin interactions
ENSG00000270268	chromatin interactions
ENSG00000078596	chromatin interactions

Extended variants
information (count: 1294 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185245800	chrX:78608044-78608045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189950819	chrX:78608061-78608062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200588479	chrX:78608214-78608215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397964208	chrX:78608225-78608226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201099622	chrX:78608226-78608227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77683538	chrX:78608227-78608228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182663067	chrX:78608283-78608284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533457375	chrX:78608310-78608311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139449385	chrX:78608350-78608351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185846471	chrX:78608639-78608640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375399795	chrX:78608672-78608673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191444704	chrX:78608695-78608696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551621105	chrX:78609025-78609026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569734444	chrX:78609115-78609116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3086651	chrX:78609152-78609153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202231784	chrX:78609154-78609155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72072283	chrX:78609162-78609163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557633290	chrX:78609163-78609164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201132476	chrX:78609172-78609173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs5902780	chrX:78609173-78609174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200204267	chrX:78609174-78609175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12556638	chrX:78609176-78609177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12556639	chrX:78609193-78609194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5912279	chrX:78609194-78609195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143847854	chrX:78609227-78609228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1040408	chrX:78609267-78609268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183326352	chrX:78609293-78609294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75810848	chrX:78609329-78609330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188729974	chrX:78609339-78609340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143802662	chrX:78609408-78609409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193074141	chrX:78609416-78609417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5912908	chrX:78609488-78609489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140953988	chrX:78609501-78609502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs5912909	chrX:78609517-78609518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76241889	chrX:78609614-78609615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369571205	chrX:78609651-78609652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5959314	chrX:78609912-78609913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548804919	chrX:78609945-78609946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1751100	chrX:78609994-78609995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1751099	chrX:78610067-78610068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183389682	chrX:78610072-78610073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1736640	chrX:78610205-78610206	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs571220977	chrX:78610209-78610210	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs186646255	chrX:78610260-78610261	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs191442320	chrX:78610382-78610383	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs111559669	chrX:78610436-78610437	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs5912280	chrX:78610514-78610515	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370302636	chrX:78610531-78610532	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148686912	chrX:78610554-78610555	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1736639	chrX:78610583-78610584	ZNF genes & repeats 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
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
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:78608000-78615000	Weak transcription	Primary T cells from cord blood	blood
2	chrX:78609000-78610600	Weak transcription	Fetal Muscle Trunk	muscle
3	chrX:78609800-78611600	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chrX:78610200-78610400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chrX:78610200-78611000	ZNF genes & repeats	Thymus	Thymus
6	chrX:78610200-78611600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chrX:78610400-78610600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
8	chrX:78610400-78611000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chrX:78610600-78610800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chrX:78610600-78611000	Strong transcription	Fetal Muscle Trunk	muscle
11	chrX:78610600-78611000	ZNF genes & repeats	Fetal Muscle Leg	muscle
12	chrX:78610600-78616600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chrX:78610800-78611000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
14	chrX:78611000-78614400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chrX:78611000-78615200	Weak transcription	Fetal Thymus	thymus
16	chrX:78611000-78618400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chrX:78611000-78618600	Weak transcription	Thymus	Thymus
18	chrX:78611000-78619200	Weak transcription	Fetal Muscle Leg	muscle
19	chrX:78611000-78620800	Weak transcription	Fetal Muscle Trunk	muscle
20	chrX:78611200-78614200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chrX:78611600-78613000	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chrX:78611600-78615400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chrX:78612200-78616200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chrX:78613000-78615200	Weak transcription	Primary T cells fromperipheralblood	blood
25	chrX:78613000-78617000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chrX:78613200-78618400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chrX:78614000-78616600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chrX:78614200-78614600	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chrX:78614200-78618200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chrX:78614400-78618600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chrX:78614600-78615600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chrX:78614600-78619800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chrX:78614800-78616400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chrX:78615000-78615600	Enhancers	Primary T cells from cord blood	blood
35	chrX:78615000-78618800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chrX:78615200-78618600	Strong transcription	Primary T cells fromperipheralblood	blood
37	chrX:78615200-78618800	Strong transcription	Fetal Thymus	thymus
38	chrX:78615400-78615600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chrX:78615400-78618400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chrX:78615600-78616000	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chrX:78615600-78616400	Weak transcription	Primary T cells from cord blood	blood
42	chrX:78615800-78618000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chrX:78616000-78616200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chrX:78616000-78616800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
45	chrX:78616200-78616800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chrX:78616200-78620800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chrX:78616200-78620800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chrX:78616400-78617200	Active TSS	Primary T cells from cord blood	blood
49	chrX:78616400-78617600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chrX:78616400-78618600	Enhancers	Primary T helper naive cells from peripheral blood	blood

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