| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00257 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:10492360-10493890 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr1:10492795-10492806 | ATGACCTTGAG | - | 6.02 | | Esrrg | MA0643.1 | chr1:10492795-10492805 | ATGACCTTGA | - | 6.02 | | GATA2 | MA0036.3 | chr1:10493663-10493674 | TTCTTATCTTT | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr1:10492360-10492375 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr1:10492694-10492715 | GGAGGAGGAGGAGGAGGAAGA | + | 11.36 | | ZNF263 | MA0528.1 | chr1:10492697-10492718 | GGAGGAGGAGGAGGAAGATCT | + | 6.01 | | ZNF263 | MA0528.1 | chr1:10492686-10492707 | GGGGGAGGGGAGGAGGAGGAG | + | 6.56 | | ZNF263 | MA0528.1 | chr1:10492691-10492712 | AGGGGAGGAGGAGGAGGAGGA | + | 9.02 |
|
| | 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 |
| GH01I010432 | chr1 | 10492532 | 10494590 |
|
Enhancer Sequence | TGAACTCCTG ACCTCAAGTG ATCTGCCCGC CTTGGCCTCC TAAAATGCTG AGATTACAGG 60
TGTGAACCAC TGTGCCCGGC CTGTTCTTAG TCCCTAGAAC AGAGCCTGGC TCTCAATAGA 120
CCAACAAATG CTTACTGATG AAGCTGCAAA GATGGGCTGA GAAATTTGCC CCTCAGCTGT 180
GATTAGCTTG TAGACGATTT CCCCCCATTC ATGTAACCAA CTGTTCTAGG CACTTGGTAG 240
GCAGCAGTGA ACAAAATTGA CAGGGTCCTG CCCTTGAGGA GTTTAGTGAT TTAGCCTCTA 300
AGTGCAGTGA TACCCCAGCC CAGCCAGGGG GAGGGGAGGA GGAGGAGGAG GAAGATCTGA 360
GAAAAATTCC TGGAGCCAAG AGCATTCAGA AGAATTCATG TCCTGTACCC TGACCCCCAC 420
CCATACCTAA AAAAGATGAC CTTGAGCCGG GCAGGGTGTT GTGGGCCTGT AGTCCCAGCT 480
ACTCAAGAGG CTGAGGCAGG AGGTTCACTT GAGCCCAGGA GTTCGAGGCT GTAGTGTGCA 540
GTGATCACAC CTGTGATCTT CGTGCCTCCC AGGTTGATGC CTCTTTGGCT TCTCCTACCA 600
GAGGCCTCAG CTTACCTAGT CTTGTGAGGT CTGAAATTCA GGAAAGTAGA TGCCCTCCTC 660
ATCTGTCTGG CCTCTATCCT GAGTTCCTGG ACTTGGGTTT TGGCAGTTCC TCCTCCTCTT 720
GCCTATGCGT TGAACACTTG CTGGTAGATT TTATGCCCTT GTGGGTTCAG CTGTCATCAC 780
GTGCAGCTCA GCTGTGTCTT CGGCCCCGAG GCGGAGTACC CACAGGTGGG CTCAACAGAA 840
CTCTGTCGAC ACGTGGCTGA GACCATTGCT TAGCTTGTCT TGCAATTGAG GCTCATCCTC 900
CCCTCTCGGT AATTTTCTGC AAGGGGTGGA GAGATCTTTT TCAGTATTGA AAAGGTTTGC 960
CAAGGAGCAG TGAGGGCCCC GTGGAGGTGG CCTCCCAACC CTCCAAATCG AGAGGGGTGG 1020
GTGTGCCCTC TTGAGCCTTT CCCGTGTTGT ACTTCTGTCC TCTGTGACGT GCAGGCCTGG 1080
GGCTGCCAGG GGCTTGCAGC AGAGGGATGG GATCCTTCTG TATTGTTGAT TAACTGCCTT 1140
AAGGGCAAAG TTCCCTGCCC GGTTTTTCAT TGTTTCCCAA ACACCTAGCA TATGCCCTTA 1200
CTGAGTTGGA GCTCTGCAGA TAGTTTGGAA TAAGTGAGTG AAACCACTCA GGGCCTTGGC 1260
AGGCATCAGT CTGACCTGTC TCCCCACTGA CTTGCCATCT AATTTCTTAT CTTTACCTGA 1320
CATAAATCAT AACCATTAAC AAGGAAGTAA TGTTTCCACA AGTCGCACTC CAGTGGGTCT 1380
CATTAACTTA TTAGTACACT TGAAAAGCCA CTCAGCCATT ATGGAAAGCG CCAGAGGGAT 1440
TGGGCTGAGC AGACCCTCTC CTTGGTCTTC ATTTTTTAAG GCGTGAAAAG CTCTTATTTG 1500
CAGCCTTACC CGTGAAATAT TTTGATGTTT 1530
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