Variant report

Variant	esv3394616
Chromosome Location	chrX:76981346-77048544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:855)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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:77041510-77042003	GM12878	blood:	n/a	chrX:77041828-77041842
6	BCL3	chrX:77041290-77041657	A549	lung:	n/a	n/a
7	BHLHE40	chrX:77041450-77042009	GM12878	blood:	n/a	n/a
8	BRCA1	chrX:77041645-77042153	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chrX:77044673-77044756	GM12878	blood:	n/a	n/a
10	BRCA1	chrX:77040875-77041075	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chrX:77041355-77041780	K562	blood:	n/a	n/a
12	CEBPB	chrX:77005268-77005612	A549	lung:	n/a	n/a
13	CEBPB	chrX:77005177-77005630	A549	lung:	n/a	n/a
14	CEBPB	chrX:76996006-76996321	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chrX:77040092-77040683	Hela-S3	cervix:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
16	CEBPB	chrX:77041064-77042056	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chrX:77005207-77005606	IMR90	lung:	n/a	n/a
18	CEBPB	chrX:77040134-77040440	K562	blood:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
19	CEBPB	chrX:76995375-76995544	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chrX:77040140-77040423	IMR90	lung:	n/a	chrX:77040269-77040280 chrX:77040269-77040280
21	CEBPB	chrX:77005233-77005612	A549	lung:	n/a	n/a
22	CEBPB	chrX:77043447-77043838	HepG2	liver:	n/a	n/a
23	CEBPD	chrX:77041509-77041753	HepG2	liver:	n/a	n/a
24	CHD1	chrX:77041101-77041802	IMR90	lung:	n/a	n/a
25	CHD1	chrX:77041317-77041807	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chrX:77041356-77042102	GM12878	blood:	n/a	n/a
27	CHD1	chrX:77040537-77040871	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chrX:77041060-77041278	GM12878	blood:	n/a	n/a
29	CHD2	chrX:77040876-77041991	Hela-S3	cervix:	n/a	n/a
30	CHD2	chrX:77041506-77041981	GM12878	blood:	n/a	n/a
31	CHD2	chrX:77040904-77041201	K562	blood:	n/a	n/a
32	CHD2	chrX:77040927-77041703	HepG2	liver:	n/a	n/a
33	CHD2	chrX:77041314-77041972	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chrX:77040966-77041073	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chrX:77041405-77041798	K562	blood:	n/a	n/a
36	CREB1	chrX:77041617-77042035	ECC-1	luminal epithelium:	n/a	n/a
37	CREB1	chrX:77041471-77042101	HepG2	liver:	n/a	n/a
38	CREB1	chrX:77041407-77042111	GM12878	blood:	n/a	n/a
39	CREB1	chrX:77005197-77005597	A549	lung:	n/a	n/a
40	CREB1	chrX:77041448-77042028	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chrX:77041412-77042048	GM12878	blood:	n/a	n/a
42	CREB1	chrX:77041684-77041980	A549	lung:	n/a	n/a
43	CREB1	chrX:77041705-77041994	ECC-1	luminal epithelium:	n/a	n/a
44	CREB1	chrX:77005233-77005541	A549	lung:	n/a	n/a
45	CREB1	chrX:77041488-77042002	A549	lung:	n/a	n/a
46	CREB1	chrX:77041382-77042093	HepG2	liver:	n/a	n/a
47	CREB1	chrX:77041550-77042024	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chrX:76987382-76987536	GM19239	blood:	n/a	n/a
49	CTCF	chrX:76987379-76987575	GM12891	blood:	n/a	n/a
50	CTCF	chrX:76987411-76987523	GM12892	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:77040152-77040202	A549	lung:	n/a
2	chrX:77040152-77040202	A549	lung:	n/a
3	chrX:77041828-77041878	AG10803	skin:	n/a
4	chrX:77042040-77042090	A549	lung:	n/a
5	chrX:77045387-77045437	GM19239	blood:	n/a
6	chrX:77042040-77042090	Hela-S3	cervix:	n/a
7	chrX:77040152-77040202	GM12891	blood:	n/a
8	chrX:77042040-77042090	T-47D	breast:	n/a
9	chrX:77042539-77042589	HL-60	blood:	n/a
10	chrX:77040152-77040202	T-47D	breast:	n/a
11	chrX:77040152-77040202	AG09319	gingival:	n/a
12	chrX:77041452-77041502	GM19239	blood:	n/a
13	chrX:77042539-77042589	HRCEpiC	kidney:	n/a
14	chrX:77041722-77041772	HIPEpiC	eye:	n/a
15	chrX:77041452-77041502	NT2-D1	testis:	n/a
16	chrX:77042539-77042589	Hela-S3	cervix:	n/a
17	chrX:77040152-77040202	HNPCEpiC	eye:	n/a
18	chrX:77042040-77042090	NH-A	brain:	n/a
19	chrX:77041745-77041795	Hepatocyte	liver:	n/a
20	chrX:77041559-77041609	AG09309	skin:	n/a
21	chrX:77041745-77041795	BJ	skin:	n/a
22	chrX:77042040-77042090	IMR90	lung:	fetal
23	chrX:77045387-77045437	LNCaP	prostate:	n/a
24	chrX:77041559-77041609	HRCEpiC	kidney:	n/a
25	chrX:77037960-77038010	PrEC	prostate:	n/a
26	chrX:77037960-77038010	MCF-7	breast:	n/a
27	chrX:77042539-77042589	HCM	heart:	n/a
28	chrX:77045387-77045437	AG09309	skin:	n/a
29	chrX:77042040-77042090	HCPEpiC	choroid plexus:	n/a
30	chrX:77040152-77040202	AG10803	skin:	n/a
31	chrX:77041722-77041772	NHBE	bronchial:	n/a
32	chrX:77041832-77041882	AoSMC	blood vessel:	n/a
33	chrX:77041722-77041772	SK-N-SH	brain:	n/a
34	chrX:77042539-77042589	U87	brain:	n/a
35	chrX:77037960-77038010	HNPCEpiC	eye:	n/a
36	chrX:77041194-77041244	ovcar-3	ovarian:	n/a
37	chrX:77040152-77040202	GM06990	blood:	n/a
38	chrX:77041832-77041882	HNPCEpiC	eye:	n/a
39	chrX:77040152-77040202	HCT-116	colon:	n/a
40	chrX:77041835-77041885	HCPEpiC	choroid plexus:	n/a
41	chrX:77041828-77041878	HRCEpiC	kidney:	n/a
42	chrX:77041452-77041502	Hela-S3	cervix:	n/a
43	chrX:77041745-77041795	AG04449	skin:	fetal
44	chrX:77041745-77041795	SK-N-MC	brain:	n/a
45	chrX:77041559-77041609	U87	brain:	n/a
46	chrX:77041194-77041244	HEEpiC	esophagus:	n/a
47	chrX:77041722-77041772	H1-hESC	embryonic stem cell:	embryo
48	chrX:77042040-77042090	AG09319	gingival:	n/a
49	chrX:77042017-77042067	PrEC	prostate:	n/a
50	chrX:77041832-77041882	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chrX:77038824..77040402-chrX:77040852..77043710,2	MCF-7	breast:
2	chrX:77034133..77037506-chrX:77038826..77043053,5	MCF-7	breast:
3	chr6:31782707..31783357-chrX:77041284..77041967,2	Hela-S3	cervix:
4	chrX:77023181..77025657-chrX:77041110..77043745,2	MCF-7	breast:
5	chr1:161146829..161147435-chrX:77041250..77041882,2	Hela-S3	cervix:
6	chrX:77038723..77041459-chrX:77150362..77152719,2	MCF-7	breast:
7	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
8	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
9	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
10	chr16:278934..279887-chrX:77040783..77041763,2	Hela-S3	cervix:
11	chrX:76996384..76998942-chrX:77041132..77042972,2	MCF-7	breast:
12	chrX:77034724..77036644-chrX:77040474..77043894,3	K562	blood:
13	chr15:90931452..90932078-chrX:77041481..77042209,2	Hela-S3	cervix:
14	chr12:6644346..6644900-chrX:77041514..77042242,2	Hela-S3	cervix:
15	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
16	chrX:77033474..77036528-chrX:77040329..77042995,4	MCF-7	breast:
17	chr17:42200945..42201659-chrX:77040836..77041635,2	Hela-S3	cervix:
18	chrX:76993528..76995377-chrX:76996626..76999172,2	MCF-7	breast:
19	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
20	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
21	chrX:76993528..76995377-chrX:76996626..76999172,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX7B-5	chrX:76983344-76983557	NONHSAT137691

No data

Variant related genes	Relation type
ATRX	TF binding region
FABP5P15	TF binding region
ATRX	CpG island
FABP5P15	CpG island
ENSG00000140575	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000085224	chromatin interactions
ENSG00000108840	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000111640	chromatin interactions
ENSG00000007392	chromatin interactions
ENSG00000102158	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190139133	chrX:76981427-76981428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182692642	chrX:76981429-76981430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143317799	chrX:76981492-76981493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371222626	chrX:76981499-76981500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563003400	chrX:76981588-76981589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530099896	chrX:76981622-76981623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187815270	chrX:76981661-76981662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111811017	chrX:76981685-76981686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192110151	chrX:76981739-76981740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376320580	chrX:76981746-76981747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184027411	chrX:76981751-76981752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367579555	chrX:76981772-76981773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371458661	chrX:76981778-76981779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187541144	chrX:76981798-76981799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192124524	chrX:76981849-76981850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542224716	chrX:76981863-76981864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184213840	chrX:76981939-76981940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368860765	chrX:76982065-76982066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187086032	chrX:76982078-76982079	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192868090	chrX:76982090-76982091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs184486908	chrX:76982126-76982127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372578584	chrX:76982306-76982307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374628517	chrX:76982323-76982324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111963837	chrX:76982388-76982389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189418581	chrX:76982389-76982390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369529932	chrX:76982609-76982610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6649996	chrX:76982613-76982614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141327516	chrX:76982722-76982723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112426978	chrX:76982840-76982841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145850132	chrX:76982931-76982932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180685696	chrX:76983013-76983014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111799474	chrX:76983134-76983135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34199296	chrX:76983170-76983171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371734897	chrX:76983172-76983173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79245951	chrX:76983211-76983212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77173335	chrX:76983214-76983215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78705511	chrX:76983243-76983244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149016623	chrX:76983268-76983269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373629597	chrX:76983270-76983271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552092256	chrX:76983453-76983454	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs56393765	chrX:76983481-76983482	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs544295883	chrX:76983508-76983509	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs200970570	chrX:76983509-76983510	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs185727244	chrX:76983620-76983621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201346107	chrX:76983695-76983696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556556140	chrX:76983726-76983727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189334960	chrX:76983950-76983951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143645546	chrX:76984017-76984018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181674946	chrX:76984103-76984104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374225339	chrX:76984164-76984165	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
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

Chromatin state (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76961000-76987400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chrX:76971600-76998800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chrX:76977000-76986000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chrX:76979800-76987000	Weak transcription	Psoas Muscle	Psoas
5	chrX:76984200-76984400	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chrX:76984400-76986600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chrX:76984800-76985200	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chrX:76985000-76985400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chrX:76985200-76986800	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chrX:76985400-76986000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chrX:76985600-76985800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chrX:76985600-76986000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chrX:76985800-76999000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chrX:76986000-76986400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chrX:76986000-76987000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chrX:76986000-77011400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chrX:76986400-76987400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chrX:76986600-76989000	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chrX:76986800-76987000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chrX:76986800-76987000	Enhancers	Stomach Mucosa	stomach
21	chrX:76986800-76987200	Weak transcription	Fetal Intestine Small	intestine
22	chrX:76986800-76988400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chrX:76987000-76987600	Enhancers	Psoas Muscle	Psoas
24	chrX:76987000-76987800	Enhancers	Primary B cells from peripheral blood	blood
25	chrX:76987000-76987800	Enhancers	Primary T cells fromperipheralblood	blood
26	chrX:76987000-76987800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chrX:76987000-76988000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chrX:76987000-76988200	Enhancers	Liver	Liver
29	chrX:76987000-76989000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chrX:76987000-76996200	Weak transcription	Stomach Mucosa	stomach
31	chrX:76987200-76987800	Enhancers	H1 Cell Line	embryonic stem cell
32	chrX:76987200-76987800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chrX:76987200-76987800	Enhancers	Esophagus	oesophagus
34	chrX:76987200-76987800	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chrX:76987200-76987800	Enhancers	Left Ventricle	heart
36	chrX:76987200-76988000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chrX:76987200-76988400	Enhancers	A549	lung
38	chrX:76987200-76988600	Enhancers	HepG2	liver
39	chrX:76987400-76987800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chrX:76987400-76987800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chrX:76987400-76987800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chrX:76987400-76987800	Enhancers	Gastric	stomach
43	chrX:76987400-76987800	Enhancers	Pancreas	Pancrea
44	chrX:76987400-76987800	Enhancers	Right Ventricle	heart
45	chrX:76987400-76987800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chrX:76987400-76988000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chrX:76987400-76988000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chrX:76987400-76988200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chrX:76987600-76987800	Enhancers	Right Atrium	heart
50	chrX:76987600-76988000	Enhancers	HUES6 Cell Line	embryonic stem cell

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