| Tag | Content |
|---|
EnhancerAtlas ID | HS059-01574 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:46391100-46392570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr1:46391724-46391738 | TCTTGTCTTGTCTT | - | 6.34 | | TCF3 | MA0522.2 | chr1:46391712-46391722 | AACACCTGCT | + | 6.02 |
|
| | 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 |
| GH01I045924 | chr1 | 46390190 | 46396649 |
|
Enhancer Sequence | GAAAATGATT CCAGAGTATT GATTGGCACT CAGATGGGGG TGTTGCATTT TTAGAGTAAG 60
AGTGCTAGAT TGACTTTGTG TTGTAAGTGG TGTCCTTGAA GAGAGGAGGC AGTTGTGTCT 120
CTGGCTATTC ACTGGCCCAG CTGTAGGCCT GCTGGAGAGA GAAGTTTGAT GTTAACAGCT 180
TAATGGAACA CAGAATGACT TAGGTTTTGA ATCAGTTTTG AATTGCCATA GACTTTGTCA 240
GCCCTGAAGT AGGAGGGCTT GCAGCAGGAA ATCCTTACTA GAGTGATTTT TATATTGGAA 300
GCATTCTAGC TTTATCTTGC TTCCTACTGC ATAGGAATTT CTTCCATACA ATGTCTAGCA 360
AAAAGCTATT CAGCCTTTGC TTGAACATCT TCAGCAACAA GCAGTTCACT CTCAAAGCTT 420
TCATCCAGTG GTACCAATTT AGTTCTCTGG CACCTCCTAT GTCACACGTA TGAGAGACTT 480
TTGGTAGACT TGCGTGGCAA ATGGACAGGT GTTCCTTTGG GCCTCCTCCA GAACTAGGCA 540
ACCTTTGAAA CCCCTTTTTG GTAGTGTCAA AATTATTTCC TGCCAAAGAG AAAGCACTAT 600
TTTCATTTTA CCAACACCTG CTTTTCTTGT CTTGTCTTTT TTTAAACAAC TGCTTTTCAG 660
AGTAATTTCA AAAGAGGAAC ATCTCCCAGA ACTTGTTCTT ATCCTGGCCC TGCTGCATAG 720
TGGTGGTAGG CAGATTACTT CACTTCTTTC TACCTCAGTT CTCTTCATTA TTAAAATGGG 780
ACTCACAATA GTATTTCAAG GATTATAGTA AGAATTAAGT GAGTCAGTAC ATCTACAATT 840
GTTTAGATAT TACCTGGGCT GCTAGACTGG TTATTTTGCT GCTTCCATTG TTGGGAGACT 900
CAGATGTTGC TAATTCTTAG CACTTCATTT TGCTTCCATT ACTTTTTTCT TTGCTTCTAT 960
TACTTTTCTC ATATTCTTAT TTTCCCTTGG ATATATTGCC TACCATATGT CCATACTGCA 1020
GAAGCTCCAT TACTGGCTTA GGTGAGGCAG TGGCAGCTGG GTGCCCTCCT GCCCTCTCAT 1080
GCATTCTCAC TAATTGTTTC TGCTGAAAAC TGGCCTGTTG GGGCTCAGCA GGACATGGAC 1140
TGAAATGAAA AACACTTTGA ATTACATTCT TTCTAAAAGA CCATTTTTTG GCAATGAGGA 1200
AAGTCCATCA AAACGGTTTC AAGGTATTTC ATTTCTCCTC TTACAGCAGG GAAAGCGCAT 1260
CTTGAGAGTA TCTTCAGAAG AAGTGATTCT CTTGTTAGAG TAGGGAAGGT TTTTTGATTT 1320
TTTTTTTTTG TTTTTTCATT GAAAAGGTAA AATAATGAAG ACTAGTGCTG TGCTTTAACT 1380
TCAGGAACCC TTATATGCGA CAGATAGTTT TTCATAGACC CTGGCTCCAG GTGACCCTGA 1440
ATGAAGATAT AATCCTGTAT GGCTAGATGC 1470
|
