Variant report

Variant	nsv1022383
Chromosome Location	chr5:103969150-104086850
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	chr5:103979079-103979393	IMR90	lung:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
2	CEBPB	chr5:104068408-104068610	HepG2	liver:	n/a	chr5:104068507-104068518
3	CEBPB	chr5:103982017-103982428	MCF-7	breast:	n/a	n/a
4	CEBPB	chr5:104021885-104022145	A549	lung:	n/a	n/a
5	CEBPB	chr5:104038023-104038389	Hela-S3	cervix:	n/a	chr5:104038323-104038334
6	CEBPB	chr5:103979047-103979334	MCF-7	breast:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
7	CEBPB	chr5:103979076-103979477	MCF-7	breast:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
8	CEBPB	chr5:103973626-103974033	HepG2	liver:	n/a	chr5:103974009-103974018 chr5:103973699-103973710 chr5:103974007-103974020
9	CEBPB	chr5:103981327-103981788	MCF-7	breast:	n/a	chr5:103981430-103981441
10	CEBPB	chr5:103979059-103979385	Hela-S3	cervix:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
11	CEBPB	chr5:103981974-103982456	MCF-7	breast:	n/a	n/a
12	CEBPB	chr5:103979071-103979419	A549	lung:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
13	CEBPB	chr5:103978060-103978382	IMR90	lung:	n/a	chr5:103978230-103978241
14	CEBPB	chr5:103979072-103979406	H1-hESC	embryonic stem cell:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
15	CEBPB	chr5:103979056-103979406	HepG2	liver:	n/a	chr5:103979192-103979204 chr5:103979237-103979250 chr5:103979238-103979249
16	CEBPB	chr5:103978093-103978388	HepG2	liver:	n/a	chr5:103978230-103978241
17	CTCF	chr5:104056791-104056829	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr5:104069820-104069970	HEK293	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
19	CTCF	chr5:104044860-104045010	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:104069820-104069970	HRE	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
21	CTCF	chr5:104069880-104070030	HCT-116	colon:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
22	CTCF	chr5:104002741-104002833	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr5:104069900-104070050	HBMEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
24	CTCF	chr5:103988002-103988060	MCF-7	breast:	n/a	n/a
25	CTCF	chr5:104016442-104016544	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr5:104069920-104070070	HPF	lung:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
27	CTCF	chr5:104083160-104083310	GM12868	blood:	n/a	n/a
28	CTCF	chr5:104069900-104070050	HRE	kidney:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
29	CTCF	chr5:104072280-104072430	BE2_C	brain:	n/a	n/a
30	CTCF	chr5:104069890-104069999	HUVEC	blood vessel:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
31	CTCF	chr5:104069900-104070050	WERI-Rb-1	eye:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
32	CTCF	chr5:104069980-104070130	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:104069903-104069973	HepG2	liver:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
34	CTCF	chr5:104003407-104003425	GM20000	blood:	n/a	n/a
35	CTCF	chr5:104069845-104070041	H1-hESC	embryonic stem cell:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
36	CTCF	chr5:104044346-104044414	GM10248	blood:	n/a	n/a
37	CTCF	chr5:104072240-104072390	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr5:104056841-104056858	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr5:103988820-103988970	GM12864	blood:	n/a	n/a
40	CTCF	chr5:104072300-104072450	BE2_C	brain:	n/a	n/a
41	CTCF	chr5:104016580-104016730	GM12870	blood:	n/a	n/a
42	CTCF	chr5:103988462-103988502	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:104069880-104070030	Hela-S3	cervix:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
44	CTCF	chr5:104056762-104056779	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr5:104083547-104083599	LNCaP	prostate:	n/a	n/a
46	CTCF	chr5:104069860-104070010	HRPEpiC	eye:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
47	CTCF	chr5:104069880-104070030	HepG2	liver:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
48	CTCF	chr5:104069820-104069970	HCT-116	colon:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959
49	CTCF	chr5:104072300-104072385	LNCaP	prostate:	n/a	n/a
50	CTCF	chr5:104069860-104070010	BE2_C	brain:	n/a	chr5:104069945-104069966 chr5:104069943-104069961 chr5:104069946-104069959

No.	Distal block	Cell Line	Cell type
1	chr5:103950660..103952781-chr5:103982477..103984816,2	MCF-7	breast:
2	chr5:103987247..103989988-chr5:103992385..103995079,2	MCF-7	breast:
3	chr5:104033301..104035974-chr5:104038075..104040842,2	MCF-7	breast:
4	chr5:103985280..103987996-chr5:104035377..104038063,2	MCF-7	breast:
5	chr5:103984998..103987505-chr5:103990796..103992380,2	MCF-7	breast:
6	chr5:103812785..103815361-chr5:104049597..104051659,2	K562	blood:
7	chr5:103982040..103982621-chr5:104952113..104952873,2	MCF-7	breast:
8	chr5:104080992..104082950-chr5:104084605..104086219,2	K562	blood:
9	chr5:103985280..103987996-chr5:104035377..104038063,2	MCF-7	breast:
10	chr5:104028054..104030764-chr5:104032138..104034804,2	K562	blood:
11	chr5:104033301..104035974-chr5:104038075..104040842,2	MCF-7	breast:
12	chr5:104028054..104030764-chr5:104032138..104034804,2	K562	blood:
13	chr5:103761403..103764401-chr5:103998452..104000157,2	MCF-7	breast:
14	chr5:103987247..103989988-chr5:103992385..103995079,2	MCF-7	breast:
15	chr5:103984998..103987505-chr5:103990796..103992380,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-5	chr5:104082242-104082310	ENSG00000251574
2	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103082
3	lnc-NUDT12-5	chr5:104074998-104075113	ENSG00000251574
4	lnc-NUDT12-5	chr5:104072462-104072616	ENSG00000251574
5	lnc-NUDT12-5	chr5:104052350-104052364	NONHSAT103081
6	lnc-NUDT12-5	chr5:104075198-104075242	ENSG00000251574
7	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
8	lnc-NUDT12-5	chr5:104074955-104075113	ENSG00000251574
9	lnc-C5orf30-2	chr5:104079736-104079888	XLOC_004497
10	lnc-NUDT12-5	chr5:104074962-104075113	ENSG00000251574
11	lnc-NUDT12-5	chr5:104079393-104079555	ENSG00000251574
12	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
13	lnc-NUDT12-5	chr5:104080291-104080310	NONHSAT103088
14	lnc-NUDT12-5	chr5:104081064-104081147	NONHSAT103088
15	lnc-NUDT12-5	chr5:104079736-104079892	ENSG00000251574

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	chromatin interactions
CREB3L2	miRNA target sites

Extended variants
information (count: 1850 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576789032	chr5:103970612-103970613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73775469	chr5:103970619-103970620	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533428901	chr5:103970625-103970626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532395534	chr5:103970633-103970634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546023741	chr5:103970663-103970664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529326767	chr5:103970670-103970671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549165768	chr5:103970676-103970677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72780797	chr5:103970684-103970685	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139807735	chr5:103970690-103970691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547600671	chr5:103970720-103970721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570690541	chr5:103970732-103970733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539744257	chr5:103970752-103970753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145219025	chr5:103970796-103970797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs326240	chr5:103970812-103970813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs181753302	chr5:103970899-103970900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142091282	chr5:103970966-103970967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556357031	chr5:103977619-103977620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543812758	chr5:103977621-103977622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373972110	chr5:103977628-103977629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573875510	chr5:103977686-103977687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529366415	chr5:103977731-103977732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140547821	chr5:103977734-103977735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566971992	chr5:103977748-103977749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568251337	chr5:103977749-103977750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527491276	chr5:103977763-103977764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188972305	chr5:103977811-103977812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150466466	chr5:103977819-103977820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539386409	chr5:103977832-103977833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556105825	chr5:103977842-103977843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192521650	chr5:103977856-103977857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535527097	chr5:103977879-103977880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555055111	chr5:103977901-103977902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369442229	chr5:103977967-103977968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572257475	chr5:103977993-103977994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72782511	chr5:103978047-103978048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs557992987	chr5:103978093-103978094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373660664	chr5:103978121-103978122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543788110	chr5:103978127-103978128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7734797	chr5:103978133-103978134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113875236	chr5:103978134-103978135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10046033	chr5:103978146-103978147	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138204009	chr5:103978147-103978148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527448763	chr5:103978191-103978192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567766572	chr5:103978235-103978236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs33816	chr5:103978306-103978307	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs201772962	chr5:103978307-103978308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs33817	chr5:103978326-103978327	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs533256070	chr5:103978404-103978405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184553551	chr5:103978450-103978451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549850353	chr5:103978455-103978456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103970600-103971000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:103977600-103978400	Enhancers	Colon Smooth Muscle	Colon
3	chr5:103978400-103978800	Weak transcription	Colon Smooth Muscle	Colon
4	chr5:103978800-103979600	Enhancers	Colon Smooth Muscle	Colon
5	chr5:103979000-103979200	Enhancers	Rectal Smooth Muscle	rectum
6	chr5:103979000-103979400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:103979200-103981800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr5:103979400-103985400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:103979600-103980000	Weak transcription	Colon Smooth Muscle	Colon
10	chr5:103980000-103982600	Enhancers	Colon Smooth Muscle	Colon
11	chr5:103981400-103981600	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr5:103981800-103982000	Enhancers	Rectal Smooth Muscle	rectum
13	chr5:103982000-103982400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:103982200-103982400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr5:103982400-103982600	Enhancers	Rectal Smooth Muscle	rectum
16	chr5:103982600-103988000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr5:103985400-103986600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:103985400-103988400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:103985400-103988600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr5:103985600-103986200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr5:103985600-103986600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
22	chr5:103985600-103988200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:103985800-103986000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr5:103985800-103986200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
25	chr5:103986000-103989000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:103986200-103986400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr5:103986200-103986600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:103986400-103986600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
29	chr5:103986600-103986800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr5:103987400-103987800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr5:103987400-103988000	Enhancers	Colon Smooth Muscle	Colon
32	chr5:103987800-103988600	Enhancers	Placenta Amnion	Placenta Amnion
33	chr5:103988000-103988200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr5:103988000-103988200	Enhancers	Rectal Smooth Muscle	rectum
35	chr5:103988000-103988400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:103988000-103988800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr5:103988200-103988600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr5:103988400-103988600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:103988400-103988600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:103988400-103988600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:103988400-103988600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
42	chr5:103988600-103988800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:103988600-103988800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr5:103988600-103989000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:103988600-103989000	ZNF genes & repeats	Spleen	Spleen
46	chr5:103988600-103990200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr5:103988800-103989000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:103992000-103992200	Enhancers	Rectal Smooth Muscle	rectum
49	chr5:103992200-103995200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr5:103992400-103996400	Weak transcription	Colon Smooth Muscle	Colon

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