| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01805 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:56998310-56999040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:56998529-56998541 | AAGTAAACAGAC | + | 6.52 | | FOXP2 | MA0593.1 | chr1:56998529-56998540 | AAGTAAACAGA | + | 6.32 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_28250 | chr1:56997761-56998865 | Fetal_Intestine | | SE_28999 | chr1:56997779-56999080 | Fetal_Intestine_Large | | SE_32719 | chr1:56997253-56998648 | H1 | | SE_40732 | chr1:56994573-57004538 | Left_Ventricle | | SE_42379 | chr1:56997630-56998723 | Lung |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I056532 | chr1 | 56998101 | 57003835 |
|
Enhancer Sequence | ATTTTAAGGA AGAAAACAGG ACATTTTCCC CTGCTCTGTG AATCCTCTGA TATCTTTTGA 60
CCTAATGCTT TTGATTTTCT GCCCCCAGTT TATGGCCTCT TCTGTGATTT TTCACAAACA 120
TATATTGAGC ACCAAGGTCT ATGTCTCACA CTAGCAATAC CAAATCAAAT CAGATCTGTC 180
TCTCCCCTGT GCAGCTAACA GGGTAGCCAA GAAATATACA AGTAAACAGA CATGACAATC 240
AGCACAGTGA CTGCAGCCAC AGAGGTGGGC CCAGGGTTCT CTGTGACCTT TGGAAGGTGG 300
GGGAGGAGAC AGCTACGGAA TGCTTCCTGG AGAAATGTCC GCCTGGTGTT TAAGTACCTA 360
CCATGTGCCC AGAGGAAAAG ACCTGGCCCC GTCTTCCAGC AACCTATTAT GTAGCTTTTT 420
TTTTTTTTCT TTTTGATACG TGGTCTCATC CTGTCGCCCA GGCTGGAGTG CAGTGGCATG 480
ATCTTGGCTC ACTGCAATAT CCACCCCCTG GATTCAAGCG ATTCTCCTGC CTCAGTCTCC 540
CAAGTAGCTG GAATTACAGG CACATGCCAC CAAGCCCAGC TTATTTTTAT ACTTTTAGTA 600
GAGACAGGTT TTCACCATGT TGACCAGGCT GGTCTCGGAC TCCTGACCTC AAGTGATCCA 660
CCTGCCTTGG CCTATGACAG TTTGTATTAA GGTGTTATTT GCCTGCTCGA GATGGGGTAG 720
CTGCTAAGTT 730
|
