| Tag | Content |
|---|
EnhancerAtlas ID | HS180-19979 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr17:16032410-16033770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr17:16032636-16032651 | TGACCTTTGAACCCT | - | 6.99 | | NR2C2 | MA0504.1 | chr17:16032636-16032651 | TGACCTTTGAACCCT | - | 6.58 | | Nr2f6(var.2) | MA0728.1 | chr17:16032636-16032651 | TGACCTTTGAACCCT | - | 6.1 | | Nr2f6 | MA0677.1 | chr17:16032636-16032650 | TGACCTTTGAACCC | - | 6.87 | | Rxra | MA0512.2 | chr17:16032636-16032650 | TGACCTTTGAACCC | - | 7.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 16032575 | 16032829 | | chr17 | 16032882 | 16033504 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I016128 | chr17 | 16032289 | 16033939 |
|
Enhancer Sequence | GTCAATGGCT TTTCTAACAC TCGCCACTCA ATCAACATAA CATCTCACAG TTAAAATACT 60
TTTAGGTCAT GGCCATTAAA CTCCCCACAT GCAAAATCAC AATTGCCTCC TCATTAGCAG 120
TGGGCACTGC TTTGCCTCCT AGATCCTAAA ATCAGAAAGT CTTCTCTCCA ACTACAACCA 180
CCCATCGCAC ACCTTCATTG TGTCTGATCC TGCTTTGTCC TCATTGTGAC CTTTGAACCC 240
TTATTCTATC AAATTTTCAC AGTCCAGTGA GAACTGTACC TACTATTCTA CTTGCTAAAG 300
CATTTCAATA CCATGATTCC TTCACTTGCT TTATCTGACC TTCCTAACTT CTCACCCTGG 360
CTAACTGCCA GTTCCTCTTT CTTCTGGATA TTTATTGCTA GAGAAAACTG ATAAACTAGG 420
GAGATTTTAA AATTTAAACT TTCAAACCAT GAGTAGGTCT GCTTTATAAT TGGGCAAGTT 480
TTACTCAGCT CTGACTCCCT GGGACACTAC AGTGGTCACA AGACCTGTTT AAATGCTAAT 540
AACCTAACCC TGTAACCAAT GTAGCATCCA TGTGTCACTC TGAACCAGTA AGATGGCATA 600
GTAAGGACAA ATCATGCCCT TTGCCTAGCA AGTGAGCTGT GTAACCCAGA AAACGGTTTA 660
TGGCCTAAAG ATACGACGGG GACATGTCAA CTCAGCAGAA CGTAAGGAAA GAAATTCAGT 720
ATCCCCTTAG AGTTGGGTAA CACATGCTAA TCTTATTTCC CCAATACTTT TCTGCTTCTA 780
ATGCCAATCA GAGCTTCAAA GTAATCCCAC GCATTCCCTG CTGTCTAAAA TCCAACCAAC 840
AGATAACTTC ACTCCCCTTT CCCTGGTGCT AGGGAATAAG AAACAACTGC AGCACCTGCT 900
TAAACCAATC AGTGTAAAGA AGGAAACAGC TCCTGGCTCT GCATAGTGTG GAAATGATCC 960
AAAGAAATGG ACAGAGTTGC TGCATTAGAG TCTAGAGAAG TGTTTGGTAC CTGTCCAGCA 1020
GAACCTCTCA CCCCTCTGTA TACTGACCAG GCAGTGGTGA GCGGAGAGGA AGTGCAGTCA 1080
GCAGCAACTG GAGGACCTCA CCTTTGTGCA ATATGCATAA AGACCTATCA TAACAACTGC 1140
CACTGACATT CAAGAGAGTA AGGAATTACC TCTAATTTAA ACAAGAGATG CTTGGAACTA 1200
CTTTTGTTTC AGGCAAATCT GTAAAGAGAA GTGCCAGTCA ATCCACATGG TCTAGGATGA 1260
AGGTTACAAG TTACATCCCT CAACTCCACA GGGTGGCTGG AGCAAAAGAG GTCCACCCCT 1320
TCAAAAGAAA CCCTTCTAAA AGTTCCCTAC ACAGACACAA 1360
|
