| Tag | Content |
|---|
EnhancerAtlas ID | HS180-25222 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:9970060-9971500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:9970237-9970249 | GTTTGTTTGTTT | + | 6.32 | | IRF1 | MA0050.2 | chr2:9971102-9971123 | AAGTGGTTTCAGTTTCAGTTA | + | 6.62 | | IRF8 | MA0652.1 | chr2:9971106-9971120 | GGTTTCAGTTTCAG | - | 6.49 | | IRF9 | MA0653.1 | chr2:9971106-9971121 | GGTTTCAGTTTCAGT | - | 6.51 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26755 | chr2:9970491-9973090 | Esophagus | | SE_64906 | chr2:9970407-9971570 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 9970154 | 9971368 | | chr2 | 9970502 | 9970961 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I009829 | chr2 | 9970041 | 9972970 |
|
Enhancer Sequence | GAGACCTCTT TCTCAGAGCC AGCCTTTCTT CCATTTATTC TGTTGAGACT GGATGCTGGG 60
TGGATGTCAT TCTGGTTTCT AGTCCCCATC ATCCTGGGGG TTCATCCATA TTTTGGATCT 120
CTTGCTTCCT GATATCTTGG TCCATGTGTT CTTTTCTTGG TTACTCCCTT GTTTTTTGTT 180
TGTTTGTTTT TTGTTTTGTT TGTTTGAGAT GGAGTCTCGC TCTGTCACCA GACTGGAGTA 240
CAGAGGCGCA ATCTCGGCTC ACTGCAACCT CCGCCTCCCA GGTTCAAGTG ATTCTCCTGC 300
CTCAGCCTCC TGAGTAGCTG GGACTACAGG CACACACCAA CATGCCCAGC TAATTTTTGT 360
ATTTTTATTA GAGACGGGGT TTCACCATGT TGACCAGGCT GGTCTCAAAC TCCTGACCTT 420
GTGATCCACC CACCTCGGTC TCCCAAAGTG CTGGGATTAC AGGCGTGAGT CACTGTGCCC 480
AGCCCTAGAC TTTTATTTAA AATGAGACTT CTGTGGCTCT GTTACTCTCC TTCCTGGAAG 540
GGAGGGAGGA GCAAGACCGG TTTGCCCCAA GCCTATAAAT GGAATAAACC AGTCCCCAAC 600
AGGTTCTGCA ACTTGCCTGA GATCTTATCG CTCCTGAGTT TGGGAAACTC TTGAGTTATT 660
TAAGCCACAC TCTTAGAAGG TTGTTTTGCT TCTGTTTAAT TGGGGCTGTG CCTTCTGGCT 720
GTTGAGCTCC TTTGACAAAG TGATTTTGCA TCCAGAGTAC TTTATTCATT CATCCATTCA 780
TTCACTAAAA AAACCTTTAT TAAGCACTTG GTCTGTTAGC AGAAAAAGTA GGCTCTTTGG 840
AACAGGCAGA ACTGAGTTAA GTTCCCTCTT GGCCTCTTGC TGGTTGGGTG ACCTGATTAG 900
TCCTCCTGAG CCTCAGTTTC CTTTACTGTT TAATGACAAC AGTTAAGAGA TCATTTGGGT 960
AATGGGCCTG GTACAGTGCC TGACAGAGTC TGTGCCTAGC AAATACGCAC TCCTTATCCT 1020
TCCCCAGGGC TATGCAAACT GCAAGTGGTT TCAGTTTCAG TTATGGGCAG ACCAGGCTAC 1080
CAGCAGGCCT TGGAGCGCCT GGAGGATCCA TTCAGAGGGC AAGTGCTGGA TACTCTCTTC 1140
TCTCTAGCAG GAACATGGAG GGTGGATGAG AAGCAGCAAG GATGATGTTT GCTTTCTGGA 1200
TCATCCCTGT GCCTTGTGAT TAGCATTTAA TAGGCTCCCA GAAAGCTTTG AAGATAATCA 1260
TATGTCTACC CCTCCCTTTT GACTGATGAT CTTGACGTGA TATACGCTTA TGTCAGTGAG 1320
GAAATAGGGA GGCTCTTGCA ATGAGCCAAG AGTTGCTCTT TAGCTTTCAA AAACGTAAAG 1380
TCTAGTGAAA ATTCAGCCCA CAATGGAGTG GCACAGGAAT TTGTCTTCAG AAATGCCTCC 1440
|
