| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01537 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:63087600-63088910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr1:63088879-63088890 | TTAATTAAAAT | - | 6.62 | | NFE2L1 | MA0089.2 | chr1:63087853-63087868 | AGAGCTGAGTCATTT | - | 6.11 | | Six3 | MA0631.1 | chr1:63087953-63087970 | CTAGCTGATACCCTTTC | - | 6.13 | | Spz1 | MA0111.1 | chr1:63087956-63087967 | GCTGATACCCT | - | 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 |
| GH01I062621 | chr1 | 63087221 | 63088707 |
|
Enhancer Sequence | TCTCTTTCGG TACTTATTGG TCTCCATTCT TTACTCCCTG TTTCCATGCC TTTTTGGTGA 60
GTGAAGCACA ATTCCCTCCC TAGGCCTGGC CACATGCCTT GCTTTGCCAA TAAGCAAACA 120
TGATGCAAAC AGAGGCTTGA AAAACATTTG CACAATTTAG TTTGCTCTCT CTCTTGAACT 180
TTTGTCAGAG CTATGAGCAC ATGACCAAGC TAGCCTGCTA GAAGATGACA GTAGAATTTG 240
AGAGACATGT CACAGAGCTG AGTCATTTCT GTCTTCCCAG TAGAAGTCAG CCTATATTAG 300
CTGATCTCAG CCAACCTCCA AACTTGTGAA TGAGCCTAGT TCACTGGAGT AGTCTAGCTG 360
ATACCCTTTC CTCTACATTG GTTGTTTACT GTCCTGTACC ACTGAAAAAA ATAGATAACA 420
TATATCTGTC AACAAATAGA ACAAATGTCT TCAAAACTAT TGTGTGGGTT TGATTTTTTT 480
TTTAAATATC TATGTATTTC TAATAATTTT GACTTCACAC ATTTTATTTA TTTATTTATT 540
TTGAGACAAG GCCTCACTTT GTCACCCAGG CTGGAATACA GTGGCATTAT AATTGCTCAC 600
TGCAGCCTCA ACCTCCTGGG CTCAAGCAAT TCTCCCGTCT CAGCCTCCCA AGTAGCTGGG 660
ACTACAGGTA TACACCAACA TGGCCGGCTA ATATTTTTTA TTTTTATAGA AACAAGGTCG 720
GCCAGGCACG GCGTCTCACG CCTGTAATCC CAGCACTTTG GGAGGCTGAG ACGGACGGAT 780
CACAAGGTTA GGAGATCGAG ACCATCTTGG CCAACACGGT GAAACCCTGT CTCTACTAAA 840
AATACAAAAA ATTAGCCAGG CATGGTGGCA GGCGCCTGTA GTCCCAGCTA CTCGGGAGGC 900
TGAGACAGGA GAATGGCATG AACCCAGGAG GCGGAGCTTA CAGTGAGCCG AGACTGTGCC 960
ACTGCACTCC AGCCTGGGTG AGAGAGCAAG ACTCAAAAAC AAAAACAAAA ACAAAAACAA 1020
AAAACCCAGA AACAAGGTCT CACCATGTTG CCCAGGCTGG TCTTGAACTC TTAGGCTCAA 1080
GCGACCCCCC AGCCTTGGCC TCCTAAAGGG CTGGGATTAC AGGCATGAGC CGACATGCCT 1140
GGCCAACACA TTTTAAATCT GTACATAAAC ACTAATGATT ACTATATCCC TACTGTAGAC 1200
AGTAATCGCT CATAAACTGA AAAAGAAAAA ACTGCCTTCT GTGTCTCATT TAGGGAAAAA 1260
TCTGTGCCTT GAATTCTACT TAATTAAAAT GGTAATCTCT TTTTTTAACT 1310
|
