| Tag | Content |
|---|
EnhancerAtlas ID | HS104-16053 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr12:124581170-124582780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr12:124582672-124582683 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr12:124582672-124582682 | AAAACAAAGG | - | 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 |
| GH12I124097 | chr12 | 124582178 | 124584411 |
|
Enhancer Sequence | GGTTCCAGCA TGTCTACGTA CCCATCCAGA AAGGGCGAAT ATTCTCTGAA TTCCCCTAAA 60
TCTTTTGGGG CTGGAGCATC CTTTGCAAAT CACCGATTCT AAGATCAGCG TTGAGGGGCA 120
CCACCAGAAC CTCATGTTCA ACCCAAACGT GGAGAAATTC CTCCTCTCTT GTTCAGAATC 180
TCACTTCTTG CTCCTCTCTC AAGTGTGCTG AGAAATCAAC ATTTTTTCTT AGTGCCTCAG 240
CTTCAGACAG AGGTTTAGGA AAGCCACCAT CACTGCCTTC TTATTTTGAC TCTCTTACCT 300
GTTCCTGTCT GTCCGTCTCA CCCAGAAGGA GGAGAGGGCC ACGGCTGGGC TAGGCCATTC 360
CCAGGTTTAG TGGGTTGATC TAGACTTCAA CCTCACGACC TTGAACGCCT GGCCCTTCCA 420
TTCTCTCACC TCTGTGTGCA ATCCTCCCTT ATGCTCCCTT AGTGAGGGGA GCCAGCCTGC 480
CAGCTGGTAG CAGCGTACAA CAACTGATCA ACAGTCCTTC CCAGCTCAGA GCCTTTTGTT 540
CCTTTCTTTG TTTAGAGACA GGGTCTTGGA TGTTGCCCAG GCTGAAGTAC AGTGGAATGG 600
TCACGGCTCA CTACAGCCTC AAACTCCCCG GCTCAAGCGA CCCTCCTACC TCAGCCTCCC 660
AAATAGCTGG GACTATAGGT GTGCACCACC ACACCTAGCT AATTTTAATT TTTTGTAGAG 720
ATGGGGTCTT GCTATGTTTC TCAGGCTGGT TTTTTTCGAA CCCCTGGCCT CAAGCAATCC 780
TCCCGCCTGG ACCTCCCATA GTGCTCAGAT TACAGACGTG AGCCACTGTG CCTGGCTCTA 840
TTTTTCTTCT TTCCCTCCCC AAGAAAGAAG ACAAGGAGAT GAGAAACCTC AGCCCTATTT 900
CTTTTTGCTC TGCAAAATCC AAGCCCCATC TTTTTCCTGT TGCCACCAAA TTGAGGGCAG 960
CCCCATGTTC CTTCACTGGC TTCTGACCCA AAACTCAGAC AAATAAGATC TTGGCATTTC 1020
GTGGGCCAAA CACAAGAGGT TTCTTTTCTT TCTTTTCTCT CCCCTGTTCC CCTTTTAAAA 1080
GTGGGCCTCG GAGGTGTTGC TTTTCCTGCT GAAAGTTCCA TCCGATTGGA TTTCATGACA 1140
GGAAATACCT TACCCACTCT CTCCCTTTCT GCCTCCGCAG TGTTCTCTCC CTTCTGTGGT 1200
ACGGCTCAGC CTGTTTTGGG CTAAGGAGGC CAGCAAGTCA AACTGAAACA ATGTATTACT 1260
TGGAGCCAGG CGTGTAAAAT GAGGATGCTT GAAGTCGAGC CCAGTGTTTT CTCTTTCCAA 1320
ATAAACCCCG ATGCCCCCAA ATGGAAAAAT CCAGCTCTCA GAACATAAGC CTGCTGGCTT 1380
CTCTCTGGCT GAAAGGTGCT GCATTTGAGC TATTAAAAGG ACTCTTTCTA TTTTGCAAAA 1440
ACCAAAGCTC CCCTTGGAGG TTTATGCTGT TCCATGGGGG ACTGTTTCTT TGCTGGATGC 1500
TGAAAACAAA GGAAACACAA CAGCGGCGCT TGCGTGTGTG ACCTCTGATG GATTCTGAGA 1560
GGCTTTGACA CGGCTTGTCT CAATGAATGC TGAGGACACT GTGAGGATGG 1610
|
