| Tag | Content |
|---|
EnhancerAtlas ID | HS180-38002 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:185587570-185588800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:185587978-185587999 | AGTCTGAAAGTGAAACCAGAT | - | 6.71 | | IRF2 | MA0051.1 | chr4:185587982-185588000 | TGAAAGTGAAACCAGATT | + | 6.66 | | PRDM1 | MA0508.2 | chr4:185588460-185588470 | GTGAAAGTGA | - | 6.02 | | STAT1 | MA0137.3 | chr4:185587802-185587813 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr4:185587799-185587813 | CAGTTTCCTGGAAA | - | 6.5 | | Zfx | MA0146.2 | chr4:185588008-185588022 | CAGGCCTGGGCCCA | - | 6.06 |
|
| | 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 |
| GH04I184666 | chr4 | 185587456 | 185588699 |
|
Enhancer Sequence | CACACCACTG CACTCCAGCC TAGGCAACAG AGTGAGACCC TGTCTCAAAA AAAATAATGG 60
CAATGTGTTT CTTCATGTTT TCAAGATGTT CCCTTAGCTT TGGACCTGTC TTTCTGTTCT 120
AGACACATCA ACCTATTCAG GACATCTTTG GCATTTGCAT CTCTAATCCT AGATACTGGG 180
ATGGCCATCC ATGTCCAGAT AGTGGTTTCT GCTCCAACAT GATTTATTTC AGTTTCCTGG 240
AAAGTGCATG AGAGGCCTTT CCATTTCAAG CCTTATCTGC AATCTCATTT CTGGATTTCT 300
GACCTTTGCT TCGGCCTTGC TTTGGGGCTT CGGTCCCAGG TCGTATCAAA GATGGCTTGT 360
TTATTGTTCC AGGCAGAGCT TCAGGGTTGG GATAATTCTA GATGTACGAG TCTGAAAGTG 420
AAACCAGATT ATTTATCTCA GGCCTGGGCC CAGGTGTAAA ACAAAGTCAG TCCAAAGGAG 480
AAACACATAG TTAGAATGGG AACACCATAT GAAGGTCTGA ATAAAAGCCA AATCCTGAGT 540
GCTTATCAAA GCAGGGGTGG GACAAGAGTC CAAACAGCAG ATGATTGACT GAAGCTCAGG 600
TAACAGGTAA TTCAGTTCAG AGCTGCTAGC GTCTTAGAGT TTCACGGCCA CCTAGAGTAA 660
AAGGCGTGGA CATGGTCACT AAAGCACTGG CATGAAAGCC AGGAACCTGA TTTCTGGATT 720
AGGGGAAGGT GGCCACAGAG ACCCAGCATG CTGTTTTCAC AAGGCTCTCG TCACCTGCCT 780
GTTTCCTGGT AGCTCAGCTG GACGTTCCTT CTCAGTCTCT CTCCCTCATC CTGTGAGAAA 840
CACAGTCACC CATCCAAACC CAAAGAATGG ACTTAGAGGC ATGGAGAACA GTGAAAGTGA 900
GACTTTTTTT TTGAGACAGA GTCTCGCTCT GTCGCCCAGG CTGGAGTGCA GTGGCACGTT 960
CTTGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCG 1020
AGTAGCTGAG ACTACAGGCG TGTGCCACCA TGCCCGGCTA AGTTTTTGTA TTTTTAGTAG 1080
AGGCGGAGTT TCACCAGGTT AGCCAGGATG GTCTTGATCC CCTGACCTTG TGATCTGCCC 1140
GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGTGCCTG GCCGAAAGTG 1200
AGACTTTTAA TAACGGCCTT ACAAGATTGG 1230
|
