| Tag | Content |
|---|
EnhancerAtlas ID | HS180-25186 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:9276980-9278640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:9278185-9278198 | GAATGTTCCGGAA | - | 6.12 | | HSF1 | MA0486.2 | chr2:9277573-9277586 | GAACTTTCTAGAA | - | 6.41 | | MYCN | MA0104.4 | chr2:9278477-9278489 | GCCCACGTGGCC | + | 6.27 | | MYCN | MA0104.4 | chr2:9278477-9278489 | GCCCACGTGGCC | - | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 9277400 | 9278000 | | chr2 | 9277097 | 9277807 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I009136 | chr2 | 9276801 | 9278718 |
|
Enhancer Sequence | TGCACTCCAG CCTGGGCAAC AAGAATGAAA CTCTGTCTCA AAAAAAAAAA AAAAAAAAGA 60
TAGCACAGTT TTACATGTTA AATGGTTAAG AAATACATAC ATACTAAAAT TAATATGGTG 120
TTTTCCTTTA AAAAGACTTG AGGCTTGTTT GAGGAAGTGG GCGTTGGGGT TGTGAGCTGG 180
GTGATCTGGA ATTGGGGGGG CATTCTAGCA CCAGAGCTGG ATGGATGTGG ATGTGACTCC 240
TAACACACCC TGTGAACGGA GGGCTGGAGG GTGCATGGGT GGGGTTGTGT GTTCCTAGGG 300
TGTGTGCGAG GGTGGGGTTG TGTGTTCCTA GGGTGCGTGC ACGGGTGTGG TTGTGTGTTC 360
CTAGGTTCTG GTCAGCCAGG TGCCATTCTC TGCATTCGCC TGGTGTTTCT GAGGACAAAA 420
TTGTGCAGAG CGAATGTGAA CTTTGAAACT CACGTTATGC TCCAATTGTT CCCTACTCTA 480
GCAATTGGGA ATTGCTATTG GAGCAATTGG AGCAATTTCA TTTTCAAAAC AAGCCGTACA 540
GCGGAACTGA AAGTATCACA TCCCTTGAGG ACTCCGGACA TGTTGGGGAA GGGGAACTTT 600
CTAGAAGGTG GCATCTGCAG ATGTCAACAT CGGCGGCGGT GCCAAGAGGG GCTTTGCAGG 660
GCCACAGGGC AGCAGCTCCA TGCAGCTGGC CCCATCCCAG GCCTGGTGAG CTCTCCTGGC 720
TGTGTACTCA GCCCTGAGCC TGATGACCAA CACCAGATGC ACAGCCTGCT GTTTACCAAG 780
CCCTCCCACC CACACCAGGG TGCCTCCTGA CAGCCTCACG GGGACAAAGT GCAGGCATCA 840
TTCGTCCACA TTTGACAGAG ATGGAAGGGG GGCTCAGAGA AGCTGATTAC TTACCCGAAG 900
ACACACAGCC TGCAAAGGGA GGTGGCACTT CCACATCCCA CGCTCTGGCT GACCCTCTGC 960
CTGTCCTCCT GTGCAGTATG TGGGGTCTCG TCACCAAGCG CTGGGATAAA CTCGAGGGGC 1020
CAGGCTCAAG GCCACGCGTC CAGAGGCAAA TGCTGCAAGA AGAGAGGTGC AGGAAACCCA 1080
GGTAACCGAA AGGCACCTGC CTCGAGTGAG CTCCCTCCAG CCCTGACACC TGTTCCTTCT 1140
TTCAGTGGAA AGGACAAGCC GCCGTCCACA CTGCGCCTTT AACAGTTACA CCCAGCGAGG 1200
CTGAGGAATG TTCCGGAACA GCCAGGATGT GGGCTTCTTT GTAGCGGGAG TGTGCCACAT 1260
GTAGTTCAAT CCTGAGTCGG AGGCCTGAGC AAGCAGCTTG CAAGATGTTT GAGGAGCTTA 1320
GCATTGACTG TGGCAGGCGG GCCATTGCTT CTATGATTAA AAAGGCCCAA CTCCCCCCTA 1380
CATCTGCCCT CGACTCTCAG GGCACACCTG GGCCCTCAGG CCGGGTGTGC TCAGCTGAGC 1440
TTGGCCATTT CTCCTCCCTC GCTCCACAGG CGCACAGGGC CAGTTGGTCA TCATGCAGCC 1500
CACGTGGCCT TTGGGACCAA CCCTGCCCTG CTGGGATATG CTTCAGGGAC CTGAGGATGG 1560
AACACTCCCC TGGGCCAGTG GACAGACACA CACACACACA CACACACACA CACACACACA 1620
CACAGAAGCA AAAACTGCTT TGTCCAAGAA AGGCACAGAC 1660
|
