Variant report

Variant	nsv900935
Chromosome Location	chr13:96497070-96631221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96624887-96625205	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96548454-96548878	K562	blood:	n/a	n/a
3	ARID3A	chr13:96517464-96517648	K562	blood:	n/a	n/a
4	ATF1	chr13:96608880-96609099	K562	blood:	n/a	n/a
5	ATF3	chr13:96608777-96609107	K562	blood:	n/a	n/a
6	BACH1	chr13:96602381-96602390	K562	blood:	n/a	n/a
7	BCL11A	chr13:96606653-96606944	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr13:96608842-96609006	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr13:96516087-96516280	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr13:96612468-96612822	K562	blood:	n/a	n/a
11	CBX3	chr13:96502134-96502436	K562	blood:	n/a	n/a
12	CCNT2	chr13:96608827-96609027	K562	blood:	n/a	n/a
13	CCNT2	chr13:96525602-96525816	K562	blood:	n/a	n/a
14	CCNT2	chr13:96589983-96590394	K562	blood:	n/a	n/a
15	CEBPB	chr13:96534445-96534665	K562	blood:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
16	CEBPB	chr13:96611029-96611416	MCF-7	breast:	n/a	chr13:96611218-96611229
17	CEBPB	chr13:96510866-96511223	IMR90	lung:	n/a	n/a
18	CEBPB	chr13:96534378-96534690	A549	lung:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
19	CEBPB	chr13:96534347-96534610	Hela-S3	cervix:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
20	CEBPB	chr13:96576859-96577151	A549	lung:	n/a	n/a
21	CEBPB	chr13:96510502-96511314	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:96506907-96507136	A549	lung:	n/a	n/a
23	CEBPB	chr13:96611042-96611399	HepG2	liver:	n/a	chr13:96611218-96611229
24	CEBPB	chr13:96534394-96534706	ECC-1	luminal epithelium:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
25	CEBPB	chr13:96518101-96518321	K562	blood:	n/a	n/a
26	CEBPB	chr13:96611144-96611383	K562	blood:	n/a	chr13:96611218-96611229
27	CEBPB	chr13:96611078-96611376	Hela-S3	cervix:	n/a	chr13:96611218-96611229
28	CEBPB	chr13:96611159-96611304	H1-hESC	embryonic stem cell:	n/a	chr13:96611218-96611229
29	CEBPB	chr13:96608866-96609174	K562	blood:	n/a	n/a
30	CEBPB	chr13:96534415-96534695	ECC-1	luminal epithelium:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
31	CEBPB	chr13:96608843-96609152	K562	blood:	n/a	n/a
32	CEBPB	chr13:96506900-96507179	HepG2	liver:	n/a	n/a
33	CEBPB	chr13:96606699-96606848	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr13:96548136-96548357	K562	blood:	n/a	n/a
35	CEBPB	chr13:96506930-96507159	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:96611067-96611397	IMR90	lung:	n/a	chr13:96611218-96611229
37	CEBPB	chr13:96608817-96609167	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr13:96534371-96534687	HepG2	liver:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
39	CEBPB	chr13:96510910-96511114	A549	lung:	n/a	n/a
40	CEBPB	chr13:96576838-96577215	IMR90	lung:	n/a	n/a
41	CEBPB	chr13:96590049-96590235	K562	blood:	n/a	n/a
42	CEBPB	chr13:96598328-96598528	HepG2	liver:	n/a	chr13:96598419-96598428 chr13:96598418-96598429 chr13:96598419-96598428
43	CEBPB	chr13:96626133-96626333	HepG2	liver:	n/a	chr13:96626229-96626240
44	CEBPB	chr13:96576845-96577168	HepG2	liver:	n/a	n/a
45	CEBPB	chr13:96534354-96534695	IMR90	lung:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
46	CEBPB	chr13:96576845-96577189	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:96514815-96515026	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:96510929-96511193	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:96624895-96625170	HepG2	liver:	n/a	n/a
50	CEBPB	chr13:96611108-96611320	A549	lung:	n/a	chr13:96611218-96611229

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96583751-96583801	MCF10A-Er-Src	breast:	n/a
2	chr13:96583751-96583801	MCF10A-Er-Src	breast:	n/a
3	chr13:96583751-96583801	AG04450	lung:	fetal
4	chr13:96583885-96583935	NHDF-neo	bronchial:	n/a
5	chr13:96583751-96583801	Caco-2	colon:	n/a
6	chr13:96624108-96624158	GM06990	blood:	n/a
7	chr13:96583970-96584020	ovcar-3	ovarian:	n/a
8	chr13:96583751-96583801	Jurkat	blood:	n/a
9	chr13:96583751-96583801	MCF-7	breast:	n/a
10	chr13:96624108-96624158	AoSMC	blood vessel:	n/a
11	chr13:96583885-96583935	HRCEpiC	kidney:	n/a
12	chr13:96583970-96584020	GM12891	blood:	n/a
13	chr13:96624108-96624158	AG09309	skin:	n/a
14	chr13:96583970-96584020	Hepatocyte	liver:	n/a
15	chr13:96583751-96583801	PFSK-1	brain:	n/a
16	chr13:96624108-96624158	HCT-116	colon:	n/a
17	chr13:96583751-96583801	HRE	kidney:	n/a
18	chr13:96624108-96624158	HepG2	liver:	n/a
19	chr13:96583751-96583801	AG04449	skin:	fetal
20	chr13:96581176-96581226	SK-N-MC	brain:	n/a
21	chr13:96581176-96581226	AG09319	gingival:	n/a
22	chr13:96583885-96583935	ovcar-3	ovarian:	n/a
23	chr13:96581176-96581226	NH-A	brain:	n/a
24	chr13:96583751-96583801	HEK293	kidney:	embryo
25	chr13:96583885-96583935	RPTEC	kidney:	n/a
26	chr13:96583751-96583801	RPTEC	kidney:	n/a
27	chr13:96583885-96583935	GM06990	blood:	n/a
28	chr13:96583751-96583801	H1-hESC	embryonic stem cell:	embryo
29	chr13:96583970-96584020	SK-N-MC	brain:	n/a
30	chr13:96583970-96584020	CMK	blood:	n/a
31	chr13:96583885-96583935	GM19239	blood:	n/a
32	chr13:96583970-96584020	SK-N-SH_RA	brain:	n/a
33	chr13:96583970-96584020	T-47D	breast:	n/a
34	chr13:96583885-96583935	IMR90	lung:	fetal
35	chr13:96581176-96581226	HEEpiC	esophagus:	n/a
36	chr13:96583751-96583801	HPAEpiC	pulmonary alveolar:	n/a
37	chr13:96583751-96583801	SK-N-SH_RA	brain:	n/a
38	chr13:96581176-96581226	ECC-1	luminal epithelium:	n/a
39	chr13:96583970-96584020	BE2_C	brain:	n/a
40	chr13:96583970-96584020	AG10803	skin:	n/a
41	chr13:96624108-96624158	A549	lung:	n/a
42	chr13:96583885-96583935	ECC-1	luminal epithelium:	n/a
43	chr13:96581176-96581226	BJ	skin:	n/a
44	chr13:96624108-96624158	NHBE	bronchial:	n/a
45	chr13:96583885-96583935	HCF	heart:	n/a
46	chr13:96583885-96583935	H1-hESC	embryonic stem cell:	embryo
47	chr13:96624108-96624158	PFSK-1	brain:	n/a
48	chr13:96581176-96581226	Caco-2	colon:	n/a
49	chr13:96583885-96583935	NHBE	bronchial:	n/a
50	chr13:96583970-96584020	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:96566533..96568077-chr9:100747317..100749032,2	MCF-7	breast:
2	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
3	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
4	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
5	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
6	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
7	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
8	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
9	chr13:96512925..96513630-chr7:95036382..95037036,2	MCF-7	breast:
10	chr13:96534402..96536224-chr13:96544660..96547266,2	K562	blood:
11	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
12	chr13:96534402..96537608-chr13:96544660..96547266,3	K562	blood:
13	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
14	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
15	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
16	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
17	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-3	chr13:96567601-96567944	ENSG00000237822.1
2	lnc-DZIP1-3	chr13:96568212-96568330	ENSG00000237822.1
3	lnc-DZIP1-9	chr13:96622724-96623119	NONHSAT034781
4	lnc-DZIP1-9	chr13:96629582-96629877	NONHSAT034781

Variant related genes	Relation type
UGGT2	TF binding region
UGGT2	CpG island
ENSG00000102595	chromatin interactions

Extended variants
information (count: 4970 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4970 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3099362	chr13:96497070-96497071	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575528433	chr13:96497078-96497079	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs544356084	chr13:96497126-96497127	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs553444961	chr13:96497130-96497131	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs149577746	chr13:96497181-96497182	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs545659928	chr13:96497199-96497200	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556025998	chr13:96497221-96497222	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs192246838	chr13:96497277-96497278	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs183556156	chr13:96497311-96497312	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs540311911	chr13:96497330-96497331	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs73556783	chr13:96497350-96497351	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530091988	chr13:96497365-96497366	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs35541302	chr13:96497425-96497426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370760660	chr13:96497429-96497430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs59463809	chr13:96497433-96497434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187444158	chr13:96497478-96497479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574724539	chr13:96497492-96497493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113801679	chr13:96497499-96497500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552930165	chr13:96497568-96497569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563566836	chr13:96497581-96497582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569565170	chr13:96497585-96497586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540147530	chr13:96497587-96497588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548761893	chr13:96497616-96497617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372255473	chr13:96497631-96497632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59153773	chr13:96497632-96497633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200469015	chr13:96497633-96497634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568153110	chr13:96497678-96497679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375673079	chr13:96497679-96497680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192221190	chr13:96497730-96497731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570388818	chr13:96497735-96497736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539025644	chr13:96497748-96497749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556086778	chr13:96497768-96497769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575891380	chr13:96497834-96497835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536644611	chr13:96497851-96497852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541627324	chr13:96497889-96497890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531959248	chr13:96497899-96497900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372817671	chr13:96497918-96497919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540404350	chr13:96497951-96497952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571455313	chr13:96497956-96497957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560610581	chr13:96497959-96497960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532594715	chr13:96497973-96497974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs8001999	chr13:96497992-96497993	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs563187293	chr13:96498002-96498003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370884542	chr13:96498027-96498028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182574217	chr13:96498040-96498041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562110090	chr13:96498044-96498045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527870841	chr13:96498054-96498055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143942019	chr13:96498063-96498064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376161959	chr13:96498071-96498072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368417180	chr13:96498080-96498081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2011 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96476000-96502600	Weak transcription	Fetal Heart	heart
2	chr13:96478000-96498200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:96478000-96502600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:96478000-96502600	Weak transcription	Left Ventricle	heart
5	chr13:96478000-96568400	Weak transcription	Placenta	Placenta
6	chr13:96478200-96502200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr13:96478200-96502600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr13:96478200-96502600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr13:96478200-96502600	Weak transcription	Aorta	Aorta
10	chr13:96478200-96502600	Weak transcription	Fetal Stomach	stomach
11	chr13:96478200-96502600	Weak transcription	Gastric	stomach
12	chr13:96478200-96502600	Weak transcription	Ovary	ovary
13	chr13:96486400-96502400	Weak transcription	Osteobl	bone
14	chr13:96486400-96502600	Weak transcription	Hela-S3	cervix
15	chr13:96486400-96502600	Weak transcription	NHLF	lung
16	chr13:96486400-96503000	Weak transcription	NHDF-Ad	bronchial
17	chr13:96486600-96502200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr13:96486600-96502200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr13:96486600-96502400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:96486600-96502400	Weak transcription	HMEC	breast
21	chr13:96486600-96502600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr13:96486600-96502600	Weak transcription	NH-A	brain
23	chr13:96487000-96510000	Weak transcription	HUVEC	blood vessel
24	chr13:96490400-96502200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:96491000-96502200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr13:96491600-96500200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:96492200-96500000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr13:96493600-96502200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr13:96493800-96497800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr13:96493800-96498000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr13:96493800-96502200	Weak transcription	Fetal Muscle Leg	muscle
32	chr13:96493800-96502400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr13:96493800-96502600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr13:96493800-96502600	Weak transcription	Pancreas	Pancrea
35	chr13:96494000-96498800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:96494000-96500200	Weak transcription	HSMM	muscle
37	chr13:96494200-96501200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr13:96494600-96499000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr13:96495000-96502200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr13:96495000-96590800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr13:96495400-96498800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:96495400-96499000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:96495800-96502200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr13:96495800-96502400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr13:96495800-96502600	Weak transcription	Adipose Nuclei	Adipose
46	chr13:96496200-96502600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:96496800-96497400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr13:96496800-96497400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
49	chr13:96496800-96498800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr13:96496800-96502600	Weak transcription	Brain Substantia Nigra	brain

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