| Tag | Content |
|---|
EnhancerAtlas ID | HS180-36499 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:69828400-69829880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr4:69829325-69829342 | GAGCACATAATGTTCTC | + | 6.03 | | NR3C1 | MA0113.3 | chr4:69829325-69829342 | GAGCACATAATGTTCTC | - | 6.13 | | NR3C1 | MA0113.3 | chr4:69829325-69829342 | GAGCACATAATGTTCTC | + | 6.24 | | NR3C2 | MA0727.1 | chr4:69829325-69829342 | GAGCACATAATGTTCTC | - | 6.13 | | NR3C2 | MA0727.1 | chr4:69829325-69829342 | GAGCACATAATGTTCTC | + | 6.33 |
|
| | 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 |
| GH04I068962 | chr4 | 69828641 | 69829894 |
|
Enhancer Sequence | AGTCTAATGT ATAGAGAAAT TGTGCCAAAC ATTAACCTTT TGTTTTTCTG CTGTCTCTAC 60
ATAAATGCCT TTATTAAATA TCTGTTTTCT TTCATAGATA CAGAAGCTTA GCTTATCTTC 120
AATGCTGCCT CCTTAAACAG ATATGAGAAA CATTTGTTTA ACTGAACTCA TCTAGTCTCA 180
GGCCTAGAAC ACTGACTAAA TAGATATAGG ATGATATATT TAAGTTTGCT CTTCTTATTT 240
AACTGAATCT GTCTTTCTAA AAACCTATAG TCTATTGTTC ACTTAAGTGC TGTACTAGAA 300
CTGTGGGTGA GAATATTAAC ATCTTTGTTA TACAACCATG AGTACATGCA GATAGCTGCA 360
TAGCAGTGAT TTCCCTCCTA TTTCCCTGTG ATTAAATCCT TAACTATGCT CCTATCAGCA 420
GGAAGAAACT AGATTGATTT TCACGCTTTT TTATCTCTAT GTCCACAAAC TTAAGAATAA 480
GATGTATGAA AGCCAAAAGA GATATTAAAA TCACCTTTGC AAAAATTATA TCAGTGTGTA 540
ACCAAGCAGC TTAGCTTCAA ACCACATTTT AAAAACTTTT TTATTTCCTC TTTCTCTCCA 600
GTCTCAAGAC ACAGCTTTCC AACAATCAAC AGATGTGTAT TCTTTCATCT TGAAATAGAG 660
CATGAGAATG TGCTTTAAAA CTCCACTCTC CTTTCCCACT TTAAGCTCCC ATGCCTTCTG 720
CACATTAATT TACCTAGATG CCTGTTAAGC ACACACCATG ATAACTTATC TGACTATATA 780
CCGGTTAGAA GCTTCAGGGA TCAAATCCTA ACATGCTGCA GGCATTTCTG GAATTCTCTT 840
CCCAACAGGA GATTACTTCA AGGCTGGAGT TCACTCCCAG TTAGAGTAAC TGCAAGATTC 900
TCTGTGATTA ATTTGTAACC AGGTTGAGCA CATAATGTTC TCCCCTTCAC TAGATGGAAC 960
AATAATTCAA GATAAACCAC TGGAGTGTGT CACACAACCT GGCACATCCG AACCCACCTT 1020
GCCTCTTCTG CATTCCAAGC CCTTCTTCTT AAATCATTGC CCTATCTACA GAAATTGAGA 1080
AGTAGTAAAT TTTGAAAGAA GTGGTAAATT TTGAAAGTGC TTCTGGCCAC TTTCCCCTTT 1140
GCTGACAACA GTAATAAAAT TTACTGTCTT TCTTATTATA TCCTGCTTTT ACTATTTTGG 1200
CTTCTTTCTA CAAGTGGTGA GCAACCAGAC CCTCTTTTGT TACAGTGGAA GGTGACTGGA 1260
TTATGGGAGT GAAGCATTAT TGAATGATTT AGCACAATCC CCTTGGTGAT AAGTTAACTG 1320
TCACTCAGGT AATTCACACA ATAATTGGTT GCTTCAAACA GTTGGGAACA TCCCTTCTCT 1380
CTCTTGATCC CACCCTTGCC ATGTGATGCA ATGGCTCCTT CTATAAATTC CATCACGATT 1440
GTATGCTTTC TGTAGTCCTC ACCAGAAGCA GATACTGGAG 1480
|
