| Tag | Content |
|---|
EnhancerAtlas ID | HS180-05426 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr10:12490660-12491600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr10:12490846-12490857 | CTGAGTCATCC | - | 6.32 | | IRF1 | MA0050.2 | chr10:12490701-12490722 | TTTCTCTTTTACTTTTTGTTT | + | 6.53 | | JUNB | MA0490.1 | chr10:12490846-12490857 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr10:12490842-12490857 | ACGGCTGAGTCATCC | - | 6.09 |
|
| | 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 |
| GH10I012447 | chr10 | 12489898 | 12491885 |
|
Enhancer Sequence | ACATCAGATA TGTTGTTTTA GCCTCTGTGG CAGATTTTAT TTTTCTCTTT TACTTTTTGT 60
TTTTATCCTT TTGTACTATT TTTAAAGAAA GGAATGAGAA GAAATTATCC CCGGACCATT 120
CCTCCCGGTG AAAAACATGA AATGTGACTA TCCGGAAATG GAGTGTGATC ACAGGGGCAC 180
GTACGGCTGA GTCATCCAAA ACGCTGACTG TCGTGTAGGG CTCCGTGGTT TTGGTGGTTT 240
TCTTAACTTC TCTGTGCCCT GGTTACTTCA TCAATGTGAT GGAGATAATA ATCTCATCGG 300
ATGTTGTGAT TTACTGAGAT CATTCTTGTA AACACTTAGA ATAGTTCCTG GTACACAGCA 360
AGCGGTTTGT GATTGTTATT GTATGATTCT ATCCAGATTC TATTACGTCA TGTTACTATG 420
TTATGAAAGA TTCCAGTTCC TTGGTGCACT GATGTGGTCT TTGAAACTCA GAACAAATGT 480
TACCTGGGCC GATGTTACAT GAGTATTTGG CCATTAAAAT CAGATAAAGA GGCCAACCTA 540
GCAAGTTACT CTCATTGAAG TGTGGCTTGT CTGCCATCCT CATTGGGAGC ACGTAGAACC 600
TCCCCAAGCT GAGTGGGCAG GGTCCGTGTG GCTGTGTGAA GGGCCCCGTC GTCTTGTGTA 660
GCTGCTCCCG TGTTGAGAGT ATAGCATGTT GAAAACAGCC TTGGCAGGAA CCACGCTTGC 720
TGTTAACCAG CTCGTCCACT AACCAGCTGT GTATACCCTA GGTCAGGCCA GCTGTTTAAA 780
AAAAAAAAAA GTGAAGATAT TTGCTAAGAG AGTAGATCTC AAGTGCCATC ATCACACGCA 840
CACAAGGGGT GATGATGGCA GTTGATAGGT ATGTTAGCTT GATCATGGTG ATCATTTTAT 900
GATGTATACA TATATCAAAA CATCATGTTA CGATGTATAC 940
|
