| Tag | Content |
|---|
EnhancerAtlas ID | HS118-07677 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr16:89733970-89735610 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:89735275-89735288 | TTCTAGAACATTC | + | 7.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 89734060 | 89734315 | | chr16 | 89734858 | 89735409 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089668 | chr16 | 89735009 | 89735208 |
|
Enhancer Sequence | TGAAGTGGGA GGATCATTTG AGCCCAGGAA GTTGAGGCTT CAGTGAGCCA TGATCATGCC 60
ACAGCATTTC AGCCTGGGCC ACAGACCTTC AAGATCCTGT CTCAAAAAGA AAAAGGGATA 120
TCGCTCAGTG CTTAGTGCAG CTGTGGGTCA TTCGGCAGCT GACACAGATG AGGCTATGTA 180
ACGCAGCACT GCAGGCAGAG GGGGAGGCCA AGGCCTGAAT ACCCCGTCTG ACTAGCCTTA 240
GGCAGGCGAC TTGGCCTCTC TGCCTCCCCC ATCTGGTTAG CCTTGGGCAG TCGAGTTGGC 300
CTCTGTGTCT CCCCTGTTTG ACTAGCCTTG GGCAGATGGC TTGGCTTGTC TGTACCTCAG 360
TTTTGTCTGA AATATGGGTT GTCAGAGACC TATAGCAGAA GCTGCTGTGT GTCATTATTC 420
ACTGTTCTAG GGCTCAGAAC AGGCACGCGA TAAAAGCCAG CACCGTTGGC CGGGCGCATT 480
GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGTAGATCA CCTGAGGTCG 540
GGAGTTCAAG ACCAGCCTGG CCAACATGGA GAAACCCTGT CTCTACTAAT AATACAAAAA 600
TTCCCCAGGT GTGGTGGCAG GAGCCTGTAG TCCCAGTTGC TCAGGAGGCT GAGGCAGGAG 660
AATCACTTGA ACTCAGGAGG TGGAGGTTGC AGTGAGCCGA GATCACACCA CTGCACTCCA 720
GCCTGGGTGA CAGAGCGAGA CTCCGTCTCA AAAACTAAGA AGAAGATTAA TAATAAACCA 780
GCACTGCCAT TGCCAGCAGT CCATCCTACC TCGCATCCAG GTTCGTGAGC TACCAAGTGT 840
CCCCACAAAG CTGTAAAACA ACATGACCAC TGTAGTTACG TTTCTGTAAA AAGGTGACTG 900
AGTCTTCTAA CCCTGACCAC ACATATGTGT GCAGAGAGAG CCAGCTCCAT CCTGCTCTCC 960
CAGAAGCCTG AACAGCTGTG CCCTAGCTCG TAGCAGTGGC ACTCCAGGAA GGGGGCGGGC 1020
GGCTGTGCCC GAGCTCGTAG CAGTGGCACT CCAGGAAGGG GGCGGGCGGC TGTGTCTGAG 1080
CTCGTAGCAG TGGCACTCCA CGAAGGGGGT GGGCGGCTGT GCCCGAGCTT GTAGCAGTGG 1140
CACTCCAGGA AGGGGCGGCC GGCCAGCCAG GAGAGCAGCC GGTGAAGGAG CACTTTTGCT 1200
TTGTACGTGG CAACGCTCGG CAGGCTCAGC AGTTTCACAG GTCTCAGGCG TTCCTTGTAA 1260
CCTTAACAGG TTTAAGAAAA TGTGAGCAAC ATCAGACATG TCCATTTCTA GAACATTCTA 1320
ATGGATGAAG TTCTGTACAG AGGGCTTTAG CAGAATTAGA GACCTTTGGA GTGGAAATGA 1380
TGTCTCTGAA CCTTGAGCTC TGAGGCGGTT CCTGCCTGGA CGTGTGCCCT CCCTCCTTCC 1440
TTTGCTGGTC GCCCTGACAC CATCCTGCCA CGGATAGTGG AAGTGTTTCT CCTGTTTTCT 1500
TCCCTGAAAA AGGGTGTCCA GCATCAGCAA CCTTCATGGC TGAGTTGCAC ATCCCTTAAG 1560
CCCTGTAATG TTCATGGACA GTTTTGATCA CTTTTGGACT CACCCATTTT TTCTGCTAAC 1620
CATACATCTT AATTCCTTTA 1640
|
