| Tag | Content |
|---|
EnhancerAtlas ID | HS048-10892 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr13:113791680-113792770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr13:113792401-113792411 | GCACGTGACC | - | 6.02 |
|
| | 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 |
| GH13I113137 | chr13 | 113791918 | 113792810 |
|
Enhancer Sequence | CATGGGGTAT TTGGGGGGGA AGGATGGACC TGTACTGCAT CCTGATGATG CTGGTGGCTA 60
CAGAAGTCTC TCCATGTGTT GAAATTCATA GAAGTGTACA CCAAAACATT GGTTTTGCTG 120
TGTGAGAATT TTAAAAGTAA AAAAGTAAGA AGATAGTGTA TTTGCTTCCT AGGGCAACCA 180
TAACAAAGCA CTACAAACGC CTTAAAATAA CAGGGATTTA TTGTCGCAGC TTTGGAGACA 240
AGTCTGAAAT TAGGGTGTCA GCAGTGTTGG TTCCTTCTGG AGGCTCTGGG AGAGTCTCTG 300
TCCCAGGCTC TCTGCTCGCT TCCAGGAGCA CCCGGCAATC ATGGGCATCC TTGGGCTGCG 360
GACGCGTCGC TCCTGTCTCT GCTTTCATCT TCGCATGGCC TTCTCTCTCT GTGCCTCTGT 420
GTGACTTTTT CTGTCTCTTA TAAGGACTTT CTCCTTTATT TAGGGCCCAC ACTGACCCAG 480
CATGATCTCT TCTACAGCCT TGGCTTAGTT AACATCTGCA AAGACCCGAT TTCCAATTAA 540
GGTTCTATTC TGAGGCTGCA GGTGGACCTG AATTAGCAGG GAGGGCACTA TTCAACCAAC 600
TGTAGAGAGT TAAAAAACAA TAAGCCTGTG GACATTTTTT AGCGTAATCT AGGCTCTTGA 660
TGACCTGTTT TAAACTAATC AGCAATGAAT ATTTTTCAGC TAACGTAATG ACTATTGACA 720
AGCACGTGAC CCTTGTCTGA ATGTTAACTC AGGCATAGCA ACTAAAAACC ATCCATTGAC 780
CAGCTCGGGA GTAGCAAACA GAGCAAGCCA TTCTTGGTGC AACCTGTTTC TAGGTAATTA 840
ACTTGAAAAT ATTTTCAATA TTCAACAAAG ATGGTTCATT TAAGATGACT GAAGCCACAT 900
CTTCACAGAT GCAGAAGATC TGAATAGCTT TCCTCTTTAG ATTGAATAGT TCTAGAACAA 960
TTCATTCCTA AAAGTGACTT CCATTGGGGA AAATATCCTA TTCAGCTTGA GTCACTTAAT 1020
TATGGTTGTT ATTGGTATAA AATGTCTCTG TTTTCCCTAA TATATTTTTA AATTTCTTTT 1080
TTCCTTTTAG 1090
|
