| Tag | Content |
|---|
EnhancerAtlas ID | HS180-22992 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr18:56074430-56075800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr18:56075064-56075075 | ATATTTACTTA | - | 6.14 | | Foxq1 | MA0040.1 | chr18:56074894-56074905 | TATTGTTTATA | + | 6.32 |
|
| | 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 |
| GH18I058406 | chr18 | 56074075 | 56076162 |
|
Enhancer Sequence | GATGCTGAAT TTTTTAAAGA GTTTCTGTTA TTAAAGGATT TTAGATATTA AGTTGTAACA 60
TACAGTCATG CACCACATAG ACATCTCAGT CAGCAATGGA CTCCCATAGA CGATGGTGGA 120
CCCGTGAGAT GATAATGGAG CTGAAAAATT CCTGTTGCCT ACTCATGTTG CCTAGTGACA 180
TCATAGCCTT TGCAACCCAT CACCCTTTCT ATGTTTAGCT ACGCTTAGAT GCACAAACCC 240
TTATCATTGT GTTACAATTG CCTGAACAGA ACAGTCACAT GCTGTACAGG CTTGTAGCCT 300
CGGAGCAATA GGCTGGACCA TATAGCCTAG GTGTGTAGCA GGCTATGCCA TCCAGGTTTG 360
TGTGAGTACA CTCTGATGTT TGCACAACGA TGAAATCGCA TAACAACGCA TTTCTCAGAA 420
TGTGTCCCAG TTGTTAAGCA ACACATGAAC ATGACTGTAT TTAATATTGT TTATAGCAGA 480
AAGTTAGAGT TTGGGATTTG TCTTTTGAAT TCTAGTTATG TAGCTCTCTT AGCAATTCTA 540
AGACTCTGCC ACTAGGGTCA TCACCCTCCC TCACAACCCC TCTCACCATG ACCTCAACCC 600
CCATCCTGGC CCCCTCTTGC CTTCTCTGCA TTCTATATTT ACTTAGAAGA TCCTTGCTTG 660
TTCATGAGTT GAGATTGTCA GGGGGACATG CCCTCCGCAA TGTAATGAGT GTTTAAACAA 720
CAGTCAGGCC TTTGAACCCC AGGCTCCAGT TAAAAAGTAA CAGGCTAGAT ACTGAATCAA 780
TAGGAGGCAA ATATTAGCTA CGGAGGCTGA GAGAGACCGA GTTGGGAAAC ACTTGTTGCT 840
GGTGACATGC AAAGAGCAAT GGCCATACCC ACCTGAGGTC CAGGAAGCCC TGGGAGCCCC 900
ATGACCTTCG GCCTGTCATT GTCCTGCTCT ACATGTTGTA ACATTGAAGC CACCAGCCCT 960
TAATTAGCTT CTAGACCTCC CTCAGTCTGG ACTTCTGCAA TATCCCACTA AATGGTGTCC 1020
ACCTGATTTT TCCCCTTCCC AGCCATCTTA CACTCATGTG AGCCTGCTTC CAGCAAACTC 1080
TGATCTTGTC AATCTTCTGC TGGAAAATTT TCCATGACTC CCCATTGCAT TCCTGACTGG 1140
TGCGCAAGGG CATCTACCTG CTCTTTGGGA CGTGGGCAGG GGGATGGCAG ATCTCCAGGT 1200
GGTCACATCT AACCACCAAT TCCCAGTCTT CTTTCTCCCC CGTAGTGTGC TGCCTTCAGT 1260
GTTATCGATG ATTTCTTCTG TCTTGATACT GTGTCTTTGG TTTCCATGAC ATTTCAATCT 1320
TCTGGTTACT CTCTCACTCT TCAAATACTC CTACTATTTT TTCTCCTCTC 1370
|
