Variant report

Variant	esv15299
Chromosome Location	chr1:228716554-228744099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:367)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:228743385-228743565	HepG2	liver:	n/a	n/a
2	ATF3	chr1:228743369-228743629	K562	blood:	n/a	n/a
3	CBX3	chr1:228744029-228745432	K562	blood:	n/a	n/a
4	CBX3	chr1:228724692-228724968	K562	blood:	n/a	n/a
5	CREB1	chr1:228743297-228743744	HepG2	liver:	n/a	n/a
6	CTCF	chr1:228743450-228743522	MCF-7	breast:	n/a	n/a
7	CTCF	chr1:228743446-228743496	GM12892	blood:	n/a	n/a
8	CTCF	chr1:228733191-228733243	K562	blood:	n/a	n/a
9	CTCF	chr1:228743422-228743543	HepG2	liver:	n/a	n/a
10	CTCF	chr1:228743430-228743518	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:228733162-228733246	K562	blood:	n/a	n/a
12	CTCF	chr1:228724597-228724659	GM20000	blood:	n/a	n/a
13	EP300	chr1:228743341-228743647	GM12878	blood:	n/a	chr1:228743408-228743424
14	EP300	chr1:228733702-228735463	ECC-1	luminal epithelium:	n/a	n/a
15	EP300	chr1:228717155-228720082	ECC-1	luminal epithelium:	n/a	n/a
16	EP300	chr1:228740204-228741148	ECC-1	luminal epithelium:	n/a	n/a
17	EP300	chr1:228731337-228732427	ECC-1	luminal epithelium:	n/a	n/a
18	EP300	chr1:228732607-228733581	ECC-1	luminal epithelium:	n/a	n/a
19	EP300	chr1:228731287-228733586	ECC-1	luminal epithelium:	n/a	n/a
20	EP300	chr1:228741844-228742310	ECC-1	luminal epithelium:	n/a	n/a
21	EP300	chr1:228728789-228729257	ECC-1	luminal epithelium:	n/a	n/a
22	EP300	chr1:228722017-228722688	ECC-1	luminal epithelium:	n/a	n/a
23	EP300	chr1:228728641-228730261	ECC-1	luminal epithelium:	n/a	n/a
24	EP300	chr1:228722792-228723695	ECC-1	luminal epithelium:	n/a	n/a
25	EP300	chr1:228740270-228740984	ECC-1	luminal epithelium:	n/a	n/a
26	EP300	chr1:228734343-228735094	ECC-1	luminal epithelium:	n/a	n/a
27	EP300	chr1:228741231-228742773	ECC-1	luminal epithelium:	n/a	n/a
28	EP300	chr1:228717244-228719938	ECC-1	luminal epithelium:	n/a	n/a
29	ESR1	chr1:228741838-228742119	ECC-1	luminal epithelium:	n/a	n/a
30	ESR1	chr1:228732767-228733385	ECC-1	luminal epithelium:	n/a	n/a
31	ESR1	chr1:228731660-228732144	ECC-1	luminal epithelium:	n/a	n/a
32	ESR1	chr1:228732691-228733479	ECC-1	luminal epithelium:	n/a	n/a
33	ESR1	chr1:228717694-228718085	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr1:228731638-228732154	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:228732737-228733214	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr1:228718670-228719359	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr1:228725901-228726116	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr1:228734360-228735036	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr1:228734376-228735041	ECC-1	luminal epithelium:	n/a	n/a
40	ESR1	chr1:228731689-228732157	ECC-1	luminal epithelium:	n/a	n/a
41	ESR1	chr1:228719006-228719331	ECC-1	luminal epithelium:	n/a	n/a
42	ESR1	chr1:228718104-228718546	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr1:228734428-228734789	ECC-1	luminal epithelium:	n/a	n/a
44	ESR1	chr1:228718630-228719395	ECC-1	luminal epithelium:	n/a	n/a
45	ESR1	chr1:228718989-228719376	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr1:228731486-228732151	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr1:228732628-228733487	ECC-1	luminal epithelium:	n/a	n/a
48	ESR1	chr1:228740559-228740895	ECC-1	luminal epithelium:	n/a	n/a
49	FOS	chr1:228731727-228731971	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:228731693-228731997	MCF10A-Er-Src	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228743235-228743285	ovcar-3	ovarian:	n/a
2	chr1:228743235-228743285	ovcar-3	ovarian:	n/a
3	chr1:228741351-228741401	HL-60	blood:	n/a
4	chr1:228741351-228741401	ProgFib	skin:	n/a
5	chr1:228743235-228743285	GM12878	blood:	n/a
6	chr1:228741351-228741401	HEK293	kidney:	embryo
7	chr1:228743235-228743285	Hepatocyte	liver:	n/a
8	chr1:228743235-228743285	CMK	blood:	n/a
9	chr1:228742687-228742737	BE2_C	brain:	n/a
10	chr1:228743235-228743285	HEEpiC	esophagus:	n/a
11	chr1:228743373-228743423	U87	brain:	n/a
12	chr1:228743235-228743285	MCF-7	breast:	n/a
13	chr1:228741351-228741401	AG10803	skin:	n/a
14	chr1:228741351-228741401	AG04450	lung:	fetal
15	chr1:228743373-228743423	CMK	blood:	n/a
16	chr1:228743373-228743423	RPTEC	kidney:	n/a
17	chr1:228743373-228743423	PANC-1	pancreas:	n/a
18	chr1:228741287-228741337	ECC-1	luminal epithelium:	n/a
19	chr1:228742687-228742737	PrEC	prostate:	n/a
20	chr1:228743131-228743181	HIPEpiC	eye:	n/a
21	chr1:228741287-228741337	AG10803	skin:	n/a
22	chr1:228742687-228742737	HRCEpiC	kidney:	n/a
23	chr1:228743235-228743285	GM12892	blood:	n/a
24	chr1:228743235-228743285	AG09319	gingival:	n/a
25	chr1:228743131-228743181	HMEC	breast:	n/a
26	chr1:228743373-228743423	HEK293	kidney:	embryo
27	chr1:228743373-228743423	HCPEpiC	choroid plexus:	n/a
28	chr1:228743373-228743423	PrEC	prostate:	n/a
29	chr1:228741287-228741337	BJ	skin:	n/a
30	chr1:228742687-228742737	GM12892	blood:	n/a
31	chr1:228743373-228743423	SK-N-SH	brain:	n/a
32	chr1:228741287-228741337	GM19239	blood:	n/a
33	chr1:228743235-228743285	GM06990	blood:	n/a
34	chr1:228743235-228743285	PANC-1	pancreas:	n/a
35	chr1:228741351-228741401	NHBE	bronchial:	n/a
36	chr1:228741351-228741401	NH-A	brain:	n/a
37	chr1:228743235-228743285	BE2_C	brain:	n/a
38	chr1:228742687-228742737	Hepatocyte	liver:	n/a
39	chr1:228742687-228742737	PFSK-1	brain:	n/a
40	chr1:228741287-228741337	HIPEpiC	eye:	n/a
41	chr1:228741351-228741401	HEEpiC	esophagus:	n/a
42	chr1:228741351-228741401	CMK	blood:	n/a
43	chr1:228743235-228743285	Caco-2	colon:	n/a
44	chr1:228741287-228741337	AG04449	skin:	fetal
45	chr1:228743131-228743181	HRPEpiC	eye:	n/a
46	chr1:228741351-228741401	Caco-2	colon:	n/a
47	chr1:228743131-228743181	SK-N-MC	brain:	n/a
48	chr1:228742687-228742737	H1-hESC	embryonic stem cell:	embryo
49	chr1:228741351-228741401	K562	blood:	n/a
50	chr1:228743131-228743181	ECC-1	luminal epithelium:	n/a

No data

Variant related genes	Relation type
RNA5SP19	TF binding region
DUSP5P1	TF binding region
RNA5SP19	CpG island
DUSP5P1	CpG island

Extended variants
information (count: 1089 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566384097	chr1:228716577-228716578	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12402247	chr1:228716613-228716614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139105727	chr1:228716660-228716661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546469886	chr1:228716820-228716821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574558315	chr1:228716837-228716838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541845121	chr1:228716840-228716841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555110610	chr1:228716850-228716851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10916339	chr1:228716894-228716895	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs549077325	chr1:228716907-228716908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569377626	chr1:228716942-228716943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79899058	chr1:228717005-228717006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537574887	chr1:228717071-228717072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558362537	chr1:228717076-228717077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557827715	chr1:228717084-228717085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578092902	chr1:228717090-228717091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534514132	chr1:228717092-228717093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535331863	chr1:228717104-228717105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143897204	chr1:228717181-228717182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572879234	chr1:228717193-228717194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180769336	chr1:228717257-228717258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561517124	chr1:228717259-228717260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575343528	chr1:228717353-228717354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139803125	chr1:228717358-228717359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4147254	chr1:228717393-228717394	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187360769	chr1:228717459-228717460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548296961	chr1:228717540-228717541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377119619	chr1:228717565-228717566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559966031	chr1:228717597-228717598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529145364	chr1:228717607-228717608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540192853	chr1:228717650-228717651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12062779	chr1:228717662-228717663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs192244415	chr1:228717668-228717669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75172907	chr1:228717683-228717684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183620928	chr1:228717718-228717719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562177790	chr1:228717725-228717726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531111432	chr1:228717819-228717820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12094319	chr1:228717836-228717837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs372930720	chr1:228717852-228717853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12140692	chr1:228717894-228717895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201124813	chr1:228717895-228717896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12139852	chr1:228717898-228717899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28604305	chr1:228717906-228717907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12139879	chr1:228717923-228717924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375163026	chr1:228717930-228717931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536942397	chr1:228717937-228717938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs386640026	chr1:228717950-228717951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12143324	chr1:228717951-228717952	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs139358097	chr1:228717966-228717967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12063933	chr1:228718002-228718003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12063963	chr1:228718011-228718012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228715800-228718800	Weak transcription	Fetal Heart	heart
2	chr1:228716000-228716600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
3	chr1:228716000-228717000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:228716000-228720800	Weak transcription	Left Ventricle	heart
5	chr1:228716400-228716600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:228716400-228716800	Enhancers	Lung	lung
7	chr1:228716400-228717400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:228718800-228719600	Enhancers	Fetal Heart	heart
9	chr1:228719000-228719200	Enhancers	Psoas Muscle	Psoas
10	chr1:228719400-228720800	Weak transcription	Psoas Muscle	Psoas
11	chr1:228720800-228721000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:228720800-228721600	Enhancers	Left Ventricle	heart
13	chr1:228720800-228722600	Enhancers	Psoas Muscle	Psoas
14	chr1:228721000-228722600	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr1:228722600-228725000	Weak transcription	Psoas Muscle	Psoas
16	chr1:228725000-228725200	Enhancers	Psoas Muscle	Psoas
17	chr1:228725200-228725800	Weak transcription	Psoas Muscle	Psoas
18	chr1:228725800-228726000	Enhancers	Psoas Muscle	Psoas
19	chr1:228725800-228727800	Enhancers	HSMMtube	muscle
20	chr1:228726000-228729200	Weak transcription	Psoas Muscle	Psoas
21	chr1:228727800-228732200	Weak transcription	HSMMtube	muscle
22	chr1:228728800-228729000	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:228728800-228730400	Enhancers	Left Ventricle	heart
24	chr1:228729000-228729600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr1:228729000-228733000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr1:228729200-228729600	Enhancers	Psoas Muscle	Psoas
27	chr1:228729600-228729800	Bivalent Enhancer	Psoas Muscle	Psoas
28	chr1:228729600-228730200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr1:228730600-228731200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:228731200-228731400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:228731400-228732400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr1:228731400-228733200	Enhancers	HMEC	breast
33	chr1:228731600-228731800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:228731600-228732400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:228731800-228732400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:228732000-228732800	Enhancers	NHEK	skin
37	chr1:228732200-228732600	Enhancers	HSMMtube	muscle
38	chr1:228732600-228735200	Weak transcription	HSMMtube	muscle
39	chr1:228734400-228735000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr1:228735000-228739800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:228735200-228736000	Enhancers	HSMMtube	muscle
42	chr1:228735600-228735800	Bivalent Enhancer	Psoas Muscle	Psoas
43	chr1:228737200-228737400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:228737400-228737600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:228739800-228741000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:228740000-228741000	Enhancers	HSMMtube	muscle
47	chr1:228742600-228742800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:228742600-228742800	Bivalent Enhancer	Fetal Brain Male	brain
49	chr1:228742600-228743000	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr1:228742800-228743000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell

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