| Tag | Content |
|---|
EnhancerAtlas ID | HS180-19393 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr16:86018330-86019760 |
SNPs | | Number: 5 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:86019469-86019482 | TTCTAGAACCTTC | + | 7.12 | | IRF1 | MA0050.2 | chr16:86019297-86019318 | AAAAAGAAAATGAAAAGGAAA | - | 6.2 | | IRF1 | MA0050.2 | chr16:86019303-86019324 | AAAATGAAAAGGAAAGTCAAA | - | 6.75 | | MYC | MA0147.3 | chr16:86018869-86018881 | CAGCACGTGGCC | - | 6.37 |
|
| | 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 |
| GH16I085982 | chr16 | 86015661 | 86019930 |
|
Enhancer Sequence | CTGCCTGTAA TTGCCGTGGG ACCCTAGCAG GTGACTTAGC CATGCCCTGC CTGGGTTTAC 60
CTACCTGTAA AGAGCCCTTG TAAGGATGAA AGTAGGTGGC ACAGACCAAG CATCTGTACC 120
TGGCAGACCA GTCCTTAATA AACAGGAATT ATTGTTACTA TTATCTTGAT TGACATTTTC 180
ATTTTAACGC ATAGGAAACA GGCCTGGAGA GAGGAAGTCC GTTTCGTGAT GGCTGGAGAA 240
AGGGCGTCTC CTGACCCCTC ATCCAGAGCT GTCTGTGCTT CCCTTGGCAG CAAGATGACT 300
GACGGAGCCC AGACAAAATT TTAGTTCCTT CAAAGAAGTG TTTTGCTTTC GGGGCCGTTG 360
CTCAGTAACC CTGGGGCCGC TGGCTGAAGG CAGCATAGGC ACTTCTCAAC AAGCTCTTGA 420
GTACACGCCT GGGGAGACGG GGCCTCACTG TCAGGGGGAG ACCAGCCAGG CTGCCCTCAC 480
CGCGTTCTCT CTGTCTTTCG CGGCAGCCCT GCAGTCCTGG TCCTGATGAG TGGGAGCCAC 540
AGCACGTGGC CTTGGGAACA GCTCTTAGCC ACTGGGAGTC TTGGTTTCCT TACCCGTAAT 600
ATGAACGCAG AGGCTCCGAG CTCCAAGCAT GGTCAGACTT AGTCACGTTT TCACCCTGCA 660
ATGGAGGGAT GTTTTCGAAA CATTTTTTTT GACACCGTGT CCGCCCAGGA AATACCCTGA 720
GAAAATTAGA CAACTAAATG ATATTGACTG TTCTCATGAA TTACTCCAAT AATTTGTTTT 780
TTCCTTGACC TGCAGGTTAA AGTCAGCATT CATTGATCTG CTACATAAAG TAACATTTCT 840
TCTAATTCCA AATGTAACAT GGGCTTAATT TGGAAAACCT GGAAAACAAG AGACAAACAA 900
AACGTTGGAG GGGGAAAAAA AAAAAAACCC AACAGTGTGG GGAAATTAAA AAAAAAAATC 960
CCCAAACAAA AAGAAAATGA AAAGGAAAGT CAAACATTTA TCACGAGATA GGAAGCTGTC 1020
ATAAAACTCT TGTGTTTCTT GGAAACACTG TCCTGCTCCC AGTTTGGAGG GCCATAAAAA 1080
TCTCAGGTTA TTGCCTTTGC AGATGCCCTC TGGGAGCCTG CTGGAGGAAA GTCTTCATTT 1140
TCTAGAACCT TCTACCCTTC GGATACGTAG TGACACCAAC CACGAGGTGG TCGGTGTGGA 1200
GGGGCAGCCC TGGTCTTGCA CCTCCAGCAG GTTGCATGTT CTGGACTCTG ATGGCCCAGA 1260
GGGACCCTTC TTTCTGCAAT TTTCTAGGCA ACTTGCAAGA GTTTCTTAAC CTCTGTGCCC 1320
CCTACCTTCC CCATCTGTGA AATGGGGGAT CGCCGGGGGT TGATAAATGT GAAGTCATAC 1380
ACATGGTAGT TGTTACTGGG AGTCTAACCA CACCCCAAGC ATTTTTTTTT 1430
|
