| Tag | Content |
|---|
EnhancerAtlas ID | HS048-37540 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:99101530-99102780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr9:99102165-99102176 | AATGAGTCACA | - | 6.62 | | FOXF2 | MA0030.1 | chr9:99101834-99101848 | CAAAGGTAAACAAC | + | 6.65 | | JUN(var.2) | MA0489.1 | chr9:99102234-99102248 | GGAAAATGACTCAT | + | 6.76 | | Nr2f6(var.2) | MA0728.1 | chr9:99101611-99101626 | CGATCTCTTGACCTC | - | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 99101601 | 99101681 | | chr9 | 99101831 | 99102634 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I096338 | chr9 | 99100761 | 99104151 |
|
Enhancer Sequence | TACAGGCACT CGCCACCACA CCCAGCTAAT TTCTGTATTT TTAGTAGAGA CAGGTTTTCA 60
CCATGTTGGC CAAGATGGTC TCGATCTCTT GACCTCATGA TCTGCCCGCC TCAACCTCCC 120
AAAGAGCCGG GATTACTGGC GTGAGCCATC GTGACCAGCC CCAACCTAAA TTTTTATAGA 180
TTTTAGTTTT ATTTCCTTAA TAATGATGAG ACGGTATTAG TGGCATTTTT AAAATAATGC 240
AGCATGATTT ATTTTTAAAT CATAAAAAAT AATGTAGCAT TATTTATTTT TAAAAAGAAA 300
TAATCAAAGG TAAACAACAA TAAAGCCCTT CTTCCTTTAG ACTTACTGTT GGAACGTGAG 360
TCTTTTTCAC TTTGCACTCA GGGTTTTTTA ATCAGGGAAA AAAAGTCCTA TTATTTATCT 420
CTATTCATCA ACTGTAATAT ACTAGATGTA CTTTGAACCT ATTGCAGTGA TTCAAATACT 480
AAAGAAAGTT CACCCGCTGA GTATTTTCCA AGGGCCTAAT TTGTTAACAA GAGAAGCTGT 540
CATCTCTGAC TTTGTTCATC AGAGATAGAA TTGAGGCACT GTTAATAGAT CTATTGACTG 600
TGTAAGTCCA AAGTCTGGGC TTGAATTCCC GGAGGAATGA GTCACACACA CACATTTACC 660
ACAATCTCTG ATCTTCTCCA TCGCTCCTAG TCCCAGTTAA CCAGGGAAAA TGACTCATCA 720
AGTTTCTTTC CATTAACAAG AGAAGTTAAC ATTTTGCTCT AATTCATTAA TCAGCTTTCA 780
GAACACTCAA ACCAAACTTG GTAAACAAAA AGCAATTTTA TATTACAGGC TAACACACCT 840
AATTCATTTC TTTCTCCTAT TTGGTTTACA ATCTAAAATG AATTCCACCA CATTCAAAAG 900
GGACCAATGG GAAGAAATTT GCCCTGATTC AGTGAATACA GAGCAATGTT AGTAGTGGAA 960
ATCTCACTGT TGTTTTTTGC TTTTTGTTTT TTATATGGGG TTGATGGCTT TTTTCTTGCA 1020
GATTACAGTG AGTGTCTCAT ATATTTTGGC ATCTCGTCAT ACAATACTTT TAAAAACTAG 1080
TCAAACTTGG CTGGGCGCAG TGGCTCACGT CTGTAATTCT AGCATTTTGG AAGGCCGAGG 1140
CGGGCAGATC ACGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTATC 1200
TTTACTAAAA ATACAAAAAT TAGCCGGGCA TCATGGTGGC GGGCGCCTGT 1250
|
