Variant report

Variant	esv2753974
Chromosome Location	chr13:38341331-38363450
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	CEBPB	chr13:38360015-38360350	HepG2	liver:	n/a	chr13:38360186-38360197
2	CEBPB	chr13:38352099-38352436	HepG2	liver:	n/a	n/a
3	CTCF	chr13:38343240-38343390	HFF	foreskin:	n/a	n/a
4	CTCF	chr13:38343235-38343591	IMR90	lung:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
5	CTCF	chr13:38343280-38343430	AG04450	lung:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
6	CTCF	chr13:38343380-38343530	AG09309	skin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
7	CTCF	chr13:38343260-38343410	NHDF-neo	bronchial:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
8	CTCF	chr13:38343361-38343489	MCF-7	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
9	CTCF	chr13:38343320-38343470	Hela-S3	cervix:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
10	CTCF	chr13:38343367-38343459	HepG2	liver:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
11	CTCF	chr13:38343320-38343470	HMF	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
12	CTCF	chr13:38343341-38343428	Kidney_OC	kidney:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
13	CTCF	chr13:38343280-38343430	AG10803	skin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
14	CTCF	chr13:38343334-38343485	Hela-S3	cervix:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
15	CTCF	chr13:38343240-38343390	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:38343340-38343490	MCF-7	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
17	CTCF	chr13:38343360-38343510	BE2_C	brain:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
18	CTCF	chr13:38343420-38343570	NHEK	skin:	n/a	n/a
19	CTCF	chr13:38343300-38343450	HEEpiC	esophagus:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
20	CTCF	chr13:38343360-38343510	HEEpiC	esophagus:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
21	CTCF	chr13:38343340-38343490	GM12873	blood:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
22	CTCF	chr13:38343264-38343531	H1-hESC	embryonic stem cell:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
23	CTCF	chr13:38343368-38343441	GM13977	blood:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
24	CTCF	chr13:38343320-38343470	AoAF	blood vessel:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
25	CTCF	chr13:38343320-38343470	SK-N-SH_RA	brain:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
26	CTCF	chr13:38343380-38343530	HCM	heart:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
27	CTCF	chr13:38343320-38343470	HCM	heart:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
28	CTCF	chr13:38343340-38343490	HMEC	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
29	CTCF	chr13:38343336-38343548	HepG2	liver:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
30	CTCF	chr13:38343309-38343582	MCF-7	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
31	CTCF	chr13:38343320-38343570	HFF-Myc	foreskin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
32	CTCF	chr13:38343280-38343430	BJ	skin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
33	CTCF	chr13:38343230-38343570	K562	blood:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
34	CTCF	chr13:38343340-38343490	Caco-2	colon:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
35	CTCF	chr13:38343340-38343490	HAc	cerebellar:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
36	CTCF	chr13:38343338-38343467	Pancreas_OC	pancreas:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
37	CTCF	chr13:38343380-38343530	NHEK	skin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
38	CTCF	chr13:38343240-38343390	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr13:38343227-38343575	GM12878	blood:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
40	CTCF	chr13:38343280-38343430	HBMEC	blood vessel:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
41	CTCF	chr13:38343280-38343430	NB4	blood:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
42	CTCF	chr13:38343320-38343470	AG09319	gingival:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
43	CTCF	chr13:38343340-38343490	AG04449	skin:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
44	CTCF	chr13:38343300-38343450	HBMEC	blood vessel:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
45	CTCF	chr13:38343294-38343667	MCF-7	breast:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
46	CTCF	chr13:38343260-38343410	Hela-S3	cervix:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
47	CTCF	chr13:38343340-38343490	SK-N-SH_RA	brain:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
48	CTCF	chr13:38343342-38343514	Medullo	brain:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
49	CTCF	chr13:38343360-38343510	AG09319	gingival:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403
50	CTCF	chr13:38343340-38343490	NHDF-neo	bronchial:	n/a	chr13:38343392-38343402 chr13:38343389-38343410 chr13:38343387-38343405 chr13:38343390-38343403

No.	Distal block	Cell Line	Cell type
1	chr13:38147936..38149837-chr13:38348790..38351640,2	K562	blood:
2	chr13:38343140..38343850-chr13:38619631..38620180,3	K562	blood:
3	chr13:38343014..38343885-chr13:38797054..38798104,3	MCF-7	breast:
4	chr13:38342917..38343939-chr13:39104444..39105331,4	MCF-7	breast:
5	chr13:38346843..38348685-chr13:38354184..38356149,2	K562	blood:
6	chr13:38341398..38342310-chr13:38619796..38620598,3	MCF-7	breast:
7	chr13:38346843..38348685-chr13:38354184..38356149,2	K562	blood:
8	chr13:38343183..38343822-chr13:38619567..38620143,2	MCF-7	breast:
9	chr13:38339961..38342075-chr13:38344336..38346387,2	K562	blood:
10	chr13:38339961..38342075-chr13:38344336..38346387,2	K562	blood:
11	chr13:38343321..38344120-chr13:38796936..38797829,2	K562	blood:

Variant related genes	Relation type
TRPC4	TF binding region

Extended variants
information (count: 890 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17056593	chr13:38341331-38341332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549751036	chr13:38341391-38341392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569685340	chr13:38341429-38341430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533288853	chr13:38341448-38341449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187054905	chr13:38341452-38341453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200153756	chr13:38341475-38341476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs68056641	chr13:38341476-38341477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201006638	chr13:38341489-38341490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377514809	chr13:38341491-38341492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369699395	chr13:38341493-38341494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566532711	chr13:38341521-38341522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113792566	chr13:38341542-38341543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9285117	chr13:38341637-38341638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146657535	chr13:38341663-38341664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558466857	chr13:38341664-38341665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17056596	chr13:38341671-38341672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539467055	chr13:38341683-38341684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375468480	chr13:38341685-38341686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556218785	chr13:38341713-38341714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71439733	chr13:38341723-38341724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73168484	chr13:38341724-38341725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs140305667	chr13:38341747-38341748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150342542	chr13:38341757-38341758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138022625	chr13:38341774-38341775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181316586	chr13:38341790-38341791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78137974	chr13:38341803-38341804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533056384	chr13:38341818-38341819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577904421	chr13:38341852-38341853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373775005	chr13:38341869-38341870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529203641	chr13:38341913-38341914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116057681	chr13:38341928-38341929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73168485	chr13:38341936-38341937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs535252638	chr13:38341949-38341950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11147670	chr13:38341969-38341970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs117227673	chr13:38341985-38341986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572832311	chr13:38342015-38342016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79822372	chr13:38342040-38342041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532663591	chr13:38342095-38342096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17056597	chr13:38342205-38342206	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs35999094	chr13:38342215-38342216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376058128	chr13:38342222-38342223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146027210	chr13:38342297-38342298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372512486	chr13:38342298-38342299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138550522	chr13:38342323-38342324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572032173	chr13:38342344-38342345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185391728	chr13:38342376-38342377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17056599	chr13:38342401-38342402	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs17056602	chr13:38342492-38342493	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs12429540	chr13:38342493-38342494	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs532932322	chr13:38342494-38342495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21965145	CNVD
Hirschsprung''s Disease	21712996	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Monoclonal gammopathy of undetermined significance	19135901	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
renal disease	20603712	CNVD
Tracheal agenesis	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38341000-38349800	Weak transcription	Osteobl	bone
2	chr13:38342000-38342800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr13:38342800-38349800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr13:38349600-38350200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:38349800-38351000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:38349800-38351000	Enhancers	Osteobl	bone
7	chr13:38350000-38350800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:38350000-38350800	Enhancers	NHDF-Ad	bronchial
9	chr13:38350800-38352000	Weak transcription	NHDF-Ad	bronchial
10	chr13:38350800-38354600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:38351000-38355000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr13:38351000-38355800	Weak transcription	Osteobl	bone
13	chr13:38352000-38352200	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr13:38352000-38352200	Enhancers	Stomach Smooth Muscle	stomach
15	chr13:38352000-38352200	Enhancers	NHDF-Ad	bronchial
16	chr13:38352200-38355600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr13:38352400-38354200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr13:38352600-38357200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr13:38354200-38354400	Enhancers	Stomach Smooth Muscle	stomach
20	chr13:38354200-38357200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr13:38354400-38355000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr13:38354600-38356200	Enhancers	Colon Smooth Muscle	Colon
23	chr13:38354600-38356600	Enhancers	Rectal Smooth Muscle	rectum
24	chr13:38354600-38356800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr13:38354800-38356400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:38355000-38355200	Enhancers	Stomach Smooth Muscle	stomach
27	chr13:38355000-38355800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:38355600-38356200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr13:38355600-38356600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:38355600-38357000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:38355800-38356400	Enhancers	Osteobl	bone
32	chr13:38355800-38356800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:38355800-38359600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr13:38356200-38363400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr13:38356400-38356600	Weak transcription	Osteobl	bone
36	chr13:38356600-38357600	Strong transcription	Osteobl	bone
37	chr13:38356800-38360000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr13:38357200-38357400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr13:38357200-38357400	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:38357400-38357800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr13:38357400-38360600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr13:38357600-38360000	Weak transcription	Osteobl	bone
43	chr13:38359600-38360600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr13:38360000-38361000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr13:38360000-38361800	Enhancers	Osteobl	bone
46	chr13:38360600-38360800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr13:38360600-38360800	Enhancers	NHLF	lung
48	chr13:38360600-38361000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr13:38360800-38368600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr13:38361000-38361200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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