| Tag | Content |
|---|
EnhancerAtlas ID | HS180-38710 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:60097330-60098420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr5:60097675-60097690 | TGGCCTTTGGACTCT | - | 7.58 |
|
| | 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 |
| GH05I060800 | chr5 | 60096375 | 60099634 |
|
Enhancer Sequence | CCAGCATGGG CAACAAAGTG AGCCTCCATC TCTACAAAAA AATTAAAAAA TTAGCCAGGC 60
ATGGTGGCGC ACACCTGTGG ATTCAGCTAT ACAGGAGGCT AAGGCAGGAC GATGGCTTGA 120
GCCCGGGAGG TCAAGGCTGC AGTGAGTCAT GATCGTGTCA CTGCACTCCA GCCTGGGTGA 180
CAGAACAAGA TCCTGTCTCA AAAAAAAAGA AAAAAAAATG AAGAAACTAG AACAAAGCGA 240
GCAGAAGGAA GGATAAGCAG CTTGCTGAGT CTGTTCAGTC TTTCTTCCCT TGCAGGACGC 300
TTACTCCATC TCCTCCTGCC CTTGAATGTC AGATTCCAGG CTCTTTGGCC TTTGGACTCT 360
GGGAACTTGC ACCAGTGGCC TCTCAGGGGC TCTCAGGCCT TTGGCCTCAG ACTGAGGGCT 420
GCACTGTTGG CTTCCCTAGT TTTGAGGCTT TTGAACTTGG ACTGAGTGAC ACTACTAGCT 480
TCTCTCTCTT TCTCCAGCTT GCAGATGGCC TATTGTTGAG ACTTTGCCCT GTGAGCCAAT 540
TCTCCCTAAT AAACTCTCAT ATATATATAT ATATATATAT ATATATATAT ATATATATAT 600
ATATATATAT ATATACACAC ACACACACAC ACATATATCC TATTGGTTCT GTCCCTCTGG 660
AGGACTCTAA TACAGACTTG TGAGTTTGTC AAGTGAGATT TGAAACCATT TACTTTAGGT 720
ATGGGATTGG GTCAGTACAA TTTTTCTTTT ATATCCCTTA TGTCAGTGGT TCTTAAACCT 780
GGTTGAAAAT CAGAATCACC CAGGGAGAGA TTTGGATTCA GTTAATGTTT GGGAAAATTC 840
TGATGGGCCA GGTTTGAGAA TCTTTTCTTA ATGCTTCATA AATCATTCTC AGACATGACG 900
ACACCCATGA CAACATGAGC AACAGGCATA AAATACATGA CAAAGGATTC AGTTAAAGAA 960
GGTCACTCAG GAACGATAAG GCATCTGGGT CAAGAAGGGC AGGAATAGGA GGTGCAATCA 1020
ATGCTGGAAA AGATTAATCT AGGATTTCAA AAGAACTCAC AAGAGATGTG AAATATGGGG 1080
ACAGATCTTT 1090
|
