Variant report

Variant	esv3398050
Chromosome Location	chrX:77001746-77122444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:916)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:77043457-77043765	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:77042335-77042860	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:77041605-77042036	HepG2	liver:	n/a	n/a
4	ATF1	chrX:77041653-77042058	K562	blood:	n/a	chrX:77041828-77041842
5	ATF2	chrX:77069658-77070148	GM12878	blood:	n/a	n/a
6	ATF2	chrX:77069630-77070170	GM12878	blood:	n/a	n/a
7	ATF2	chrX:77041510-77042003	GM12878	blood:	n/a	chrX:77041828-77041842
8	BCL3	chrX:77041290-77041657	A549	lung:	n/a	n/a
9	BHLHE40	chrX:77041450-77042009	GM12878	blood:	n/a	n/a
10	BRCA1	chrX:77044673-77044756	GM12878	blood:	n/a	n/a
11	BRCA1	chrX:77040875-77041075	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chrX:77041645-77042153	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chrX:77041355-77041780	K562	blood:	n/a	n/a
14	CEBPB	chrX:77050670-77050991	HepG2	liver:	n/a	n/a
15	CEBPB	chrX:77097128-77097339	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chrX:77097138-77097348	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chrX:77056953-77057267	A549	lung:	n/a	n/a
18	CEBPB	chrX:77050765-77050965	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chrX:77055861-77056078	K562	blood:	n/a	n/a
20	CEBPB	chrX:77050673-77051018	A549	lung:	n/a	n/a
21	CEBPB	chrX:77005177-77005630	A549	lung:	n/a	n/a
22	CEBPB	chrX:77050673-77050900	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chrX:77050657-77051009	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chrX:77040134-77040440	K562	blood:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
25	CEBPB	chrX:77097142-77097323	A549	lung:	n/a	n/a
26	CEBPB	chrX:77049468-77049714	A549	lung:	n/a	chrX:77049562-77049573 chrX:77049593-77049604
27	CEBPB	chrX:77050658-77051017	MCF-7	breast:	n/a	n/a
28	CEBPB	chrX:77040092-77040683	Hela-S3	cervix:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
29	CEBPB	chrX:77097135-77097331	K562	blood:	n/a	n/a
30	CEBPB	chrX:77050650-77050951	K562	blood:	n/a	n/a
31	CEBPB	chrX:77043447-77043838	HepG2	liver:	n/a	n/a
32	CEBPB	chrX:77005207-77005606	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:77049412-77049753	HepG2	liver:	n/a	chrX:77049562-77049573 chrX:77049593-77049604
34	CEBPB	chrX:77076362-77076506	K562	blood:	n/a	n/a
35	CEBPB	chrX:77041064-77042056	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chrX:77005268-77005612	A549	lung:	n/a	n/a
37	CEBPB	chrX:77057013-77057123	K562	blood:	n/a	n/a
38	CEBPB	chrX:77049427-77049760	IMR90	lung:	n/a	chrX:77049562-77049573 chrX:77049593-77049604
39	CEBPB	chrX:77050641-77051009	IMR90	lung:	n/a	n/a
40	CEBPB	chrX:77005233-77005612	A549	lung:	n/a	n/a
41	CEBPB	chrX:77050647-77051016	K562	blood:	n/a	n/a
42	CEBPB	chrX:77050702-77051025	A549	lung:	n/a	n/a
43	CEBPB	chrX:77050652-77051005	A549	lung:	n/a	n/a
44	CEBPB	chrX:77049433-77049755	Hela-S3	cervix:	n/a	chrX:77049562-77049573 chrX:77049593-77049604
45	CEBPB	chrX:77088342-77088574	IMR90	lung:	n/a	n/a
46	CEBPB	chrX:77040140-77040423	IMR90	lung:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
47	CEBPD	chrX:77041509-77041753	HepG2	liver:	n/a	n/a
48	CHD1	chrX:77040537-77040871	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chrX:77041101-77041802	IMR90	lung:	n/a	n/a
50	CHD1	chrX:77041356-77042102	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:77037960-77038010	K562	blood:	n/a
2	chrX:77037960-77038010	K562	blood:	n/a
3	chrX:77042017-77042067	MCF10A-Er-Src	breast:	n/a
4	chrX:77042017-77042067	H1-hESC	embryonic stem cell:	embryo
5	chrX:77042040-77042090	NH-A	brain:	n/a
6	chrX:77045387-77045437	GM19239	blood:	n/a
7	chrX:77040152-77040202	K562	blood:	n/a
8	chrX:77037960-77038010	NH-A	brain:	n/a
9	chrX:77041828-77041878	PFSK-1	brain:	n/a
10	chrX:77042539-77042589	LNCaP	prostate:	n/a
11	chrX:77042017-77042067	Hela-S3	cervix:	n/a
12	chrX:77037960-77038010	SK-N-SH_RA	brain:	n/a
13	chrX:77042040-77042090	GM12891	blood:	n/a
14	chrX:77037960-77038010	NHBE	bronchial:	n/a
15	chrX:77084159-77084209	HEK293	kidney:	embryo
16	chrX:77041835-77041885	HIPEpiC	eye:	n/a
17	chrX:77042040-77042090	IMR90	lung:	fetal
18	chrX:77084159-77084209	PrEC	prostate:	n/a
19	chrX:77084159-77084209	HepG2	liver:	n/a
20	chrX:77041745-77041795	PANC-1	pancreas:	n/a
21	chrX:77041194-77041244	NH-A	brain:	n/a
22	chrX:77041835-77041885	SKMC	muscle:	n/a
23	chrX:77041832-77041882	AG09309	skin:	n/a
24	chrX:77084159-77084209	HRE	kidney:	n/a
25	chrX:77045387-77045437	T-47D	breast:	n/a
26	chrX:77041194-77041244	HRCEpiC	kidney:	n/a
27	chrX:77041722-77041772	AoSMC	blood vessel:	n/a
28	chrX:77041722-77041772	PrEC	prostate:	n/a
29	chrX:77042017-77042067	HAEpiC	amniotic membrane:	n/a
30	chrX:77041835-77041885	SK-N-SH	brain:	n/a
31	chrX:77041559-77041609	SK-N-MC	brain:	n/a
32	chrX:77037960-77038010	T-47D	breast:	n/a
33	chrX:77042040-77042090	SKMC	muscle:	n/a
34	chrX:77041559-77041609	HEEpiC	esophagus:	n/a
35	chrX:77041832-77041882	HMEC	breast:	n/a
36	chrX:77041828-77041878	HCM	heart:	n/a
37	chrX:77041745-77041795	H1-hESC	embryonic stem cell:	embryo
38	chrX:77042017-77042067	GM12891	blood:	n/a
39	chrX:77040152-77040202	HL-60	blood:	n/a
40	chrX:77042539-77042589	ProgFib	skin:	n/a
41	chrX:77041835-77041885	HRCEpiC	kidney:	n/a
42	chrX:77041194-77041244	IMR90	lung:	fetal
43	chrX:77041745-77041795	HCM	heart:	n/a
44	chrX:77041835-77041885	Jurkat	blood:	n/a
45	chrX:77037960-77038010	HL-60	blood:	n/a
46	chrX:77041835-77041885	GM06990	blood:	n/a
47	chrX:77040152-77040202	HCPEpiC	choroid plexus:	n/a
48	chrX:77045387-77045437	HUVEC	blood vessel:	n/a
49	chrX:77045387-77045437	HCM	heart:	n/a
50	chrX:77037960-77038010	SK-N-SH	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:90931452..90932078-chrX:77041481..77042209,2	Hela-S3	cervix:
2	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
3	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
4	chr6:31782707..31783357-chrX:77041284..77041967,2	Hela-S3	cervix:
5	chr1:161146829..161147435-chrX:77041250..77041882,2	Hela-S3	cervix:
6	chrX:77038723..77041459-chrX:77150362..77152719,2	MCF-7	breast:
7	chr17:42200945..42201659-chrX:77040836..77041635,2	Hela-S3	cervix:
8	chr16:278934..279887-chrX:77040783..77041763,2	Hela-S3	cervix:
9	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
10	chrX:77033474..77036528-chrX:77040329..77042995,4	MCF-7	breast:
11	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
12	chrX:77038824..77040402-chrX:77040852..77043710,2	MCF-7	breast:
13	chr12:6644346..6644900-chrX:77041514..77042242,2	Hela-S3	cervix:
14	chrX:77023181..77025657-chrX:77041110..77043745,2	MCF-7	breast:
15	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
16	chrX:77034133..77037506-chrX:77038826..77043053,5	MCF-7	breast:
17	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
18	chrX:77034724..77036644-chrX:77040474..77043894,3	K562	blood:
19	chrX:77040041..77042178-chrX:77113212..77115559,2	MCF-7	breast:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MAGT1	hsa-miR-124-3p	chrX:77084561-77084554
2	MAGT1	hsa-miR-124-3p	chrX:77082022-77082015
3	MAGT1	hsa-miR-124-3p	chrX:77082016-77082037
4	MAGT1	hsa-miR-124-3p	chrX:77084555-77084574

Variant related genes	Relation type
ATRX	TF binding region
RNU6-854P	TF binding region
ATRX	CpG island
RNU6-854P	CpG island
ENSG00000111640	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000140575	chromatin interactions
ENSG00000085224	chromatin interactions
ENSG00000102158	chromatin interactions
ENSG00000108840	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000007392	chromatin interactions

Extended variants
information (count: 1054 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200118173	chrX:77001807-77001808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373064502	chrX:77001808-77001809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181677980	chrX:77001957-77001958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34233577	chrX:77002094-77002095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144601588	chrX:77002227-77002228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368095437	chrX:77002516-77002517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186017106	chrX:77002531-77002532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188818276	chrX:77002532-77002533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35491223	chrX:77002582-77002583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181249354	chrX:77002666-77002667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111843051	chrX:77002838-77002839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559503457	chrX:77002961-77002962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533027656	chrX:77003015-77003016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186278644	chrX:77003197-77003198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190796806	chrX:77003223-77003224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147884193	chrX:77003463-77003464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182647289	chrX:77003640-77003641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187303252	chrX:77003643-77003644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113290303	chrX:77003652-77003653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190804811	chrX:77003681-77003682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537039408	chrX:77003842-77003843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183000500	chrX:77004021-77004022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201725073	chrX:77004073-77004074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372281072	chrX:77004147-77004148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376727229	chrX:77004179-77004180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78977412	chrX:77004271-77004272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80273526	chrX:77004283-77004284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55800734	chrX:77004431-77004432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187334314	chrX:77004462-77004463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565113129	chrX:77004483-77004484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140495956	chrX:77004805-77004806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191864426	chrX:77004833-77004834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150439761	chrX:77004862-77004863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6621534	chrX:77005059-77005060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183004925	chrX:77005124-77005125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111395134	chrX:77005491-77005492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367601563	chrX:77005546-77005547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188090602	chrX:77005576-77005577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554307402	chrX:77005719-77005720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192372358	chrX:77005854-77005855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144796236	chrX:77005872-77005873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72628489	chrX:77005874-77005875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375439577	chrX:77005997-77005998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184356640	chrX:77006195-77006196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376657986	chrX:77006242-77006243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189586680	chrX:77006246-77006247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192477974	chrX:77006322-77006323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557812840	chrX:77006331-77006332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184699888	chrX:77006377-77006378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189065694	chrX:77006443-77006444	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
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
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

Chromatin state (count:1455 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76986000-77011400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chrX:76995800-77007400	Weak transcription	Primary hematopoietic stem cells	blood
3	chrX:76996400-77004800	Weak transcription	A549	lung
4	chrX:76996400-77022800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chrX:76996400-77032000	Weak transcription	Hela-S3	cervix
6	chrX:76996600-77011400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chrX:76998600-77011800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chrX:76999000-77003000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chrX:76999400-77008000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chrX:76999400-77011400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chrX:76999400-77011400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chrX:76999400-77024400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chrX:76999600-77002400	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chrX:76999800-77002200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chrX:76999800-77041000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chrX:77000000-77024200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chrX:77001200-77002200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chrX:77001200-77003600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chrX:77002200-77002400	Enhancers	Primary T cells fromperipheralblood	blood
20	chrX:77002400-77002800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chrX:77002400-77011600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chrX:77002600-77002800	Enhancers	Left Ventricle	heart
23	chrX:77002800-77003000	Enhancers	Primary T cells fromperipheralblood	blood
24	chrX:77003000-77011200	Weak transcription	Primary T cells fromperipheralblood	blood
25	chrX:77003800-77004000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chrX:77004800-77005400	Enhancers	A549	lung
27	chrX:77005400-77020600	Weak transcription	A549	lung
28	chrX:77006200-77017200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chrX:77006400-77020400	Weak transcription	Esophagus	oesophagus
30	chrX:77008200-77010600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chrX:77009800-77032400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chrX:77010200-77031600	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chrX:77010600-77011600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chrX:77010600-77012000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chrX:77010800-77039400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chrX:77011000-77011800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
37	chrX:77011000-77012000	ZNF genes & repeats	Fetal Muscle Leg	muscle
38	chrX:77011000-77012200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
39	chrX:77011000-77012200	ZNF genes & repeats	Fetal Stomach	stomach
40	chrX:77011000-77012200	Enhancers	Gastric	stomach
41	chrX:77011200-77011400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chrX:77011200-77011400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chrX:77011200-77011400	ZNF genes & repeats	Fetal Intestine Large	intestine
44	chrX:77011200-77011800	Enhancers	Pancreas	Pancrea
45	chrX:77011200-77012000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chrX:77011200-77012000	Enhancers	Primary T cells fromperipheralblood	blood
47	chrX:77011200-77012000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
48	chrX:77011200-77012200	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chrX:77011200-77012400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chrX:77011200-77024000	Weak transcription	Dnd41	blood

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