| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04864 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:177952180-177953740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr1:177953307-177953317 | GTTAATTGGT | - | 6.02 | | NEUROD2 | MA0668.1 | chr1:177952373-177952383 | GCCATATGGT | + | 6.02 | | TCF7L2 | MA0523.1 | chr1:177952962-177952976 | TTCCTTTCATCTTT | - | 6.1 |
|
| | 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 |
| GH01I177983 | chr1 | 177952295 | 177954050 |
|
Enhancer Sequence | GCCTGGCTGG TGACATGTGA GATCCATTTC AGAAATAAAG CACCTGTCCC CGAATTGGAT 60
GTGGAGCTAA GGTAATGCTG TGTGAGAAGC TGTTCAGCAA GGGGAAAATT CACACTAGGT 120
GAGCAATCAA TTACTGAAGA GGTTATCCAT CCCAATGCAT TCATTTTATA GCACATAAAC 180
TGAAGCCCAG AGTGCCATAT GGTTCACTGG GATCAATGCC AGGATCCGAA TCCAGGTCCC 240
CTGACTCCCA GCCCAGTGTT CATTTCTCCT CTTATAACAT CTGTTACTCC TGCTGGGCAG 300
CAGACTCCTC AGGGGCAGTG ACCCACCTCT TCCATCTTGT TCACTTAGGT ATCCCCCCAC 360
ATAGAGAGGT GACAATCAAA AATATCTGTT CGTCAATAAG TTAACCGTAC TCAGGTTAAG 420
CCGCTGTTGG TCACTCAGGT TTTATGCAGA GCTGAACATC AGAGTAAAAG GTCTCAACAG 480
AAAAAAAAAA AAATCACCAA CCCATAAATA CATGGTTTAT GATCTCTGAA AATACTAGAA 540
ACTCTAAACA CGATTTCCAG GGTGGAAGCC TTGGGAACAG CAGCCACAGA GCCTCCTCTT 600
GTGAAGAGAT CCAAGCCGGA GTTCTATTGT CATGGGGTTG GCAGGCACCA CACCCCTAGC 660
CATCTATATA GCTTGAGAGC AAAAGTTTCC ACACTGCCTC TAAGTCAGTT TTAACCAACT 720
TGAATCCTCC TCAAAATATT TAACAGCCTC TCTCCTTTTC CCAAACACTG TAACTGCTAA 780
GCTTCCTTTC ATCTTTCCAT AATCAAACCT GCCTAAAGTT TTTTAGTAAG TTGAAATCAC 840
GTGTTCTTTT GCACATTAAC AATCCATTCC ATCCCCCAGG GAACAGCCTT TGCCAGAGTA 900
TGAAGGAACT CCAAGGAGTT AGGGTTGGAA ATTGGCATTA GCCACAGCTG AAGTTAGTTT 960
TTTCAAGCAA AACCCTGTGA AGTTCTTCAT TTTGCTGAAA ACCATGTGCT GGCTTAATGC 1020
CTTTTTGTTC TGGTTGAGAC CAAATGCTTC TCAAATGAGT CTGCTAGAAG GGTCTTTAGT 1080
GAGAACTGTA TTCCCTCTTA GCATTCTTCA ATTTGCATTT GGTTTGGGTT AATTGGTTAA 1140
TGGTGAAAAT AAGTACTTAC ATCGATTGCC CCTAAATCAG GAGTTGCTGC TGCTGCTTCT 1200
GCTATATCCC ATCATGACAG CCTGCTGTTA CTCACAGCTG GCAGATACTG TAAACTGTGT 1260
TGCCACGTCA GCTGCCCAGA ACCTTTCTGC TTCAGCAGCA GTTTCCCATC GGAATGGCTT 1320
AATAGGCAGC TCCTGAGGCT GGAAACATGA TCTGACCACC ATATTGAGAA GGTCTGAAAA 1380
AAGAGGCCAC TCTCTGACAT TACAGAAACC ACACACTCCC CTTTGTATTT CTAAATGAGA 1440
GTTCCAAAGA GAACCTAACT GTTACATTGA ATTCCTAAAC AATCAGGGCA GCAAGTTAAT 1500
AATTGGGAAA AAATTCCATC GGGATTAGAC ATTGAAAAAG TGAAAATTAG GAACTCAGCA 1560
|
