Variant report

Variant	esv2752652
Chromosome Location	chr13:96059024-96181597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1267)
CpG islands
(count:672)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1267 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96146399-96146694	K562	blood:	n/a	n/a
2	ARID3A	chr13:96130801-96131169	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:96146340-96146763	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:96137375-96138176	K562	blood:	n/a	n/a
5	ARID3A	chr13:96090573-96090866	K562	blood:	n/a	n/a
6	ARID3A	chr13:96129590-96129780	K562	blood:	n/a	n/a
7	ATF2	chr13:96132243-96132785	GM12878	blood:	n/a	n/a
8	ATF2	chr13:96109557-96110047	GM12878	blood:	n/a	n/a
9	ATF2	chr13:96109477-96110062	GM12878	blood:	n/a	n/a
10	BACH1	chr13:96146450-96146650	K562	blood:	n/a	n/a
11	BACH1	chr13:96176765-96177073	K562	blood:	n/a	n/a
12	BACH1	chr13:96089900-96090195	K562	blood:	n/a	chr13:96090032-96090046
13	BATF	chr13:96124220-96124534	GM12878	blood:	n/a	n/a
14	BATF	chr13:96109534-96109917	GM12878	blood:	n/a	n/a
15	BATF	chr13:96132378-96132759	GM12878	blood:	n/a	n/a
16	BATF	chr13:96132237-96132726	GM12878	blood:	n/a	n/a
17	BATF	chr13:96124223-96124523	GM12878	blood:	n/a	n/a
18	BCL11A	chr13:96109531-96109982	GM12878	blood:	n/a	n/a
19	BHLHE40	chr13:96129484-96129770	K562	blood:	n/a	n/a
20	BHLHE40	chr13:96090412-96090857	K562	blood:	n/a	n/a
21	BHLHE40	chr13:96130743-96131154	K562	blood:	n/a	n/a
22	BHLHE40	chr13:96093245-96093455	K562	blood:	n/a	n/a
23	BHLHE40	chr13:96175892-96176102	K562	blood:	n/a	n/a
24	BHLHE40	chr13:96130747-96131130	GM12878	blood:	n/a	n/a
25	BHLHE40	chr13:96137218-96138480	K562	blood:	n/a	n/a
26	BHLHE40	chr13:96089808-96090123	K562	blood:	n/a	n/a
27	BHLHE40	chr13:96127433-96127458	K562	blood:	n/a	n/a
28	BHLHE40	chr13:96125807-96125871	GM12878	blood:	n/a	chr13:96125838-96125851 chr13:96125841-96125850 chr13:96125840-96125849 chr13:96125834-96125855 chr13:96125840-96125849
29	BHLHE40	chr13:96072864-96072868	HepG2	liver:	n/a	n/a
30	BRCA1	chr13:96064018-96064145	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr13:96071223-96071406	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr13:96111499-96111813	K562	blood:	n/a	n/a
33	CBX3	chr13:96130699-96131130	K562	blood:	n/a	n/a
34	CCNT2	chr13:96130759-96131213	K562	blood:	n/a	n/a
35	CCNT2	chr13:96129436-96129786	K562	blood:	n/a	n/a
36	CCNT2	chr13:96132580-96132773	K562	blood:	n/a	chr13:96132698-96132718
37	CCNT2	chr13:96137307-96138248	K562	blood:	n/a	n/a
38	CCNT2	chr13:96090539-96090894	K562	blood:	n/a	n/a
39	CEBPB	chr13:96129692-96129851	K562	blood:	n/a	n/a
40	CEBPB	chr13:96084414-96084731	H1-hESC	embryonic stem cell:	n/a	chr13:96084573-96084584
41	CEBPB	chr13:96157538-96157755	A549	lung:	n/a	n/a
42	CEBPB	chr13:96084448-96084675	Hela-S3	cervix:	n/a	chr13:96084573-96084584
43	CEBPB	chr13:96176485-96176810	HepG2	liver:	n/a	chr13:96176635-96176646 chr13:96176657-96176668
44	CEBPB	chr13:96171172-96171418	HepG2	liver:	n/a	chr13:96171286-96171297
45	CEBPB	chr13:96072808-96073113	HepG2	liver:	n/a	n/a
46	CEBPB	chr13:96084498-96084671	K562	blood:	n/a	chr13:96084573-96084584
47	CEBPB	chr13:96063776-96063816	K562	blood:	n/a	n/a
48	CEBPB	chr13:96146397-96146664	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:96084421-96084747	HepG2	liver:	n/a	chr13:96084573-96084584
50	CEBPB	chr13:96060888-96061024	K562	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96086098-96086148	SKMC	muscle:	n/a
2	chr13:96086098-96086148	SKMC	muscle:	n/a
3	chr13:96085241-96085291	AG04449	skin:	fetal
4	chr13:96086275-96086325	MCF10A-Er-Src	breast:	n/a
5	chr13:96086023-96086073	ProgFib	skin:	n/a
6	chr13:96085241-96085291	HUVEC	blood vessel:	n/a
7	chr13:96085969-96086019	SKMC	muscle:	n/a
8	chr13:96086098-96086148	MCF-7	breast:	n/a
9	chr13:96087962-96088012	Jurkat	blood:	n/a
10	chr13:96086249-96086299	GM06990	blood:	n/a
11	chr13:96158480-96158530	IMR90	lung:	fetal
12	chr13:96086275-96086325	Caco-2	colon:	n/a
13	chr13:96087962-96088012	ProgFib	skin:	n/a
14	chr13:96085504-96085554	HRCEpiC	kidney:	n/a
15	chr13:96158480-96158530	GM12891	blood:	n/a
16	chr13:96086023-96086073	NHBE	bronchial:	n/a
17	chr13:96086249-96086299	HMEC	breast:	n/a
18	chr13:96085504-96085554	NHBE	bronchial:	n/a
19	chr13:96089870-96089920	NH-A	brain:	n/a
20	chr13:96086098-96086148	NH-A	brain:	n/a
21	chr13:96086275-96086325	NT2-D1	testis:	n/a
22	chr13:96086182-96086232	HRE	kidney:	n/a
23	chr13:96086182-96086232	BE2_C	brain:	n/a
24	chr13:96085504-96085554	PFSK-1	brain:	n/a
25	chr13:96086275-96086325	PANC-1	pancreas:	n/a
26	chr13:96087962-96088012	Hela-S3	cervix:	n/a
27	chr13:96089870-96089920	HIPEpiC	eye:	n/a
28	chr13:96086023-96086073	GM12892	blood:	n/a
29	chr13:96086275-96086325	T-47D	breast:	n/a
30	chr13:96086275-96086325	SAEC	small airway:	n/a
31	chr13:96085241-96085291	HCPEpiC	choroid plexus:	n/a
32	chr13:96158480-96158530	PFSK-1	brain:	n/a
33	chr13:96086098-96086148	HNPCEpiC	eye:	n/a
34	chr13:96086023-96086073	AG09309	skin:	n/a
35	chr13:96086275-96086325	MCF-7	breast:	n/a
36	chr13:96086182-96086232	HCPEpiC	choroid plexus:	n/a
37	chr13:96085969-96086019	RPTEC	kidney:	n/a
38	chr13:96089870-96089920	CMK	blood:	n/a
39	chr13:96086098-96086148	GM12892	blood:	n/a
40	chr13:96087962-96088012	HEK293	kidney:	embryo
41	chr13:96085969-96086019	BJ	skin:	n/a
42	chr13:96086098-96086148	U87	brain:	n/a
43	chr13:96085241-96085291	RPTEC	kidney:	n/a
44	chr13:96087962-96088012	SKMC	muscle:	n/a
45	chr13:96085504-96085554	AG09309	skin:	n/a
46	chr13:96086182-96086232	HUVEC	blood vessel:	n/a
47	chr13:96085969-96086019	HRCEpiC	kidney:	n/a
48	chr13:96087962-96088012	NT2-D1	testis:	n/a
49	chr13:96085969-96086019	PANC-1	pancreas:	n/a
50	chr13:96086023-96086073	NH-A	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:96125206..96127161-chr13:96129356..96131300,2	K562	blood:
2	chr13:95843997..95844511-chr13:96130866..96131628,2	MCF-7	breast:
3	chr13:96178008..96180996-chr13:96185734..96188672,2	MCF-7	breast:
4	chr13:95841410..95841915-chr13:96130869..96131391,2	MCF-7	breast:
5	chr13:96119619..96122365-chr13:96309013..96311626,2	MCF-7	breast:
6	chr13:96146062..96146563-chr13:97619520..97620349,2	K562	blood:
7	chr13:96158409..96159956-chr13:96164959..96167246,2	MCF-7	breast:
8	chr13:96058665..96059376-chr13:96130506..96131218,2	MCF-7	breast:
9	chr13:96148891..96151318-chr13:96153321..96155668,2	K562	blood:
10	chr13:96164126..96166950-chr13:96172138..96174070,2	K562	blood:
11	chr13:96164126..96166950-chr13:96172138..96174070,2	K562	blood:
12	chr13:96058665..96059376-chr13:96130506..96131218,2	MCF-7	breast:
13	chr13:96168785..96171227-chr13:96172406..96174921,2	MCF-7	breast:
14	chr13:96125206..96127161-chr13:96129356..96131300,2	K562	blood:
15	chr13:95807500..95810294-chr13:96058766..96060692,2	MCF-7	breast:
16	chr13:96056383..96057194-chr13:96130599..96131185,2	MCF-7	breast:
17	chr13:96158409..96159956-chr13:96164959..96167246,2	MCF-7	breast:
18	chr13:96148891..96151318-chr13:96153321..96155668,2	K562	blood:
19	chr13:96146074..96146987-chr13:96215991..96216972,6	MCF-7	breast:
20	chr13:96168785..96171227-chr13:96172406..96174921,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-2	chr13:96149313-96149381	NONHSAT034762
2	lnc-DZIP1-2	chr13:96149313-96149379	ENSG00000223392
3	lnc-DZIP1-2	chr13:96131698-96132216	NONHSAT034762
4	lnc-DZIP1-2	chr13:96180748-96180841	NONHSAT034762
5	lnc-DZIP1-2	chr13:96131698-96132216	ENSG00000223392
6	lnc-DZIP1-2	chr13:96180746-96180841	ENSG00000223392

No data

Variant related genes	Relation type
CLDN10	TF binding region
CLDN10	CpG island
ENSG00000223392	chromatin interactions

Extended variants
information (count: 4936 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4936 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2993570	chr13:96059024-96059025	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149130344	chr13:96059060-96059061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9516580	chr13:96059130-96059131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143225119	chr13:96059197-96059198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139382838	chr13:96059224-96059225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17301019	chr13:96059225-96059226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs372367440	chr13:96059252-96059253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143310475	chr13:96059295-96059296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374722025	chr13:96059318-96059319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576135687	chr13:96059352-96059353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147101003	chr13:96059389-96059390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192611772	chr13:96059406-96059407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575406953	chr13:96059407-96059408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572203274	chr13:96059450-96059451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7328640	chr13:96059475-96059476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554949474	chr13:96059494-96059495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184951045	chr13:96059520-96059521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371989842	chr13:96059528-96059529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141209968	chr13:96059533-96059534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35813119	chr13:96059592-96059593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150736297	chr13:96059643-96059644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138807943	chr13:96059670-96059671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531841903	chr13:96059691-96059692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548242156	chr13:96059696-96059697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562133936	chr13:96059703-96059704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201652583	chr13:96059790-96059791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527941747	chr13:96059796-96059797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188129620	chr13:96059807-96059808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115760616	chr13:96059841-96059842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539640799	chr13:96059847-96059848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139051832	chr13:96059857-96059858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116764681	chr13:96059881-96059882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12877455	chr13:96059913-96059914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs180889035	chr13:96059920-96059921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183958583	chr13:96059925-96059926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149465154	chr13:96059932-96059933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113908713	chr13:96059935-96059936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114226399	chr13:96059937-96059938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189428848	chr13:96059942-96059943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182523863	chr13:96059975-96059976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576431234	chr13:96059979-96059980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35170848	chr13:96060029-96060030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs562071565	chr13:96060048-96060049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139996187	chr13:96060088-96060089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541071522	chr13:96060124-96060125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376173346	chr13:96060150-96060151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564431880	chr13:96060161-96060162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143433266	chr13:96060172-96060173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549917427	chr13:96060187-96060188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186649940	chr13:96060200-96060201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96056600-96066000	Weak transcription	Right Atrium	heart
2	chr13:96058400-96059400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:96063600-96064000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:96063600-96064000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:96063600-96064000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:96063800-96064000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr13:96063800-96064200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:96064000-96064400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr13:96064200-96064400	Enhancers	Pancreas	Pancrea
10	chr13:96064400-96067200	Weak transcription	Pancreas	Pancrea
11	chr13:96064800-96065200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr13:96065200-96071200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr13:96066000-96067400	Enhancers	Placenta	Placenta
14	chr13:96071200-96071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr13:96071200-96071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr13:96071200-96073200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr13:96071400-96072200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr13:96071600-96072600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:96072200-96073000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr13:96072400-96073600	Enhancers	Placenta	Placenta
21	chr13:96072600-96073000	Enhancers	Primary T cells from cord blood	blood
22	chr13:96072600-96073200	Enhancers	Primary hematopoietic stem cells	blood
23	chr13:96072600-96073200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:96072800-96073200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr13:96072800-96073200	Enhancers	GM12878-XiMat	blood
26	chr13:96073600-96078800	Weak transcription	Placenta	Placenta
27	chr13:96078800-96079200	Enhancers	Placenta	Placenta
28	chr13:96079000-96079200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr13:96079200-96082000	Weak transcription	Placenta	Placenta
30	chr13:96079200-96086000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr13:96081800-96082400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr13:96081800-96086000	Weak transcription	Pancreas	Pancrea
33	chr13:96082000-96082800	Enhancers	Placenta	Placenta
34	chr13:96082400-96082600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr13:96082800-96086000	Weak transcription	Placenta	Placenta
36	chr13:96083200-96083400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr13:96085200-96088000	Active TSS	Fetal Kidney	kidney
38	chr13:96085800-96086200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr13:96086000-96086200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:96086000-96086200	ZNF genes & repeats	Pancreas	Pancrea
41	chr13:96086000-96086400	Enhancers	Placenta	Placenta
42	chr13:96086200-96086800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr13:96086200-96090600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:96086200-96090600	Weak transcription	Pancreas	Pancrea
45	chr13:96089400-96090000	Enhancers	A549	lung
46	chr13:96089600-96089800	Weak transcription	Right Atrium	heart
47	chr13:96089600-96091200	Enhancers	K562	blood
48	chr13:96089800-96090000	Enhancers	Lung	lung
49	chr13:96089800-96090200	Enhancers	Left Ventricle	heart
50	chr13:96089800-96090200	Enhancers	HUVEC	blood vessel

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