| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02080 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr11:113318200-113319900 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr11:113319772-113319786 | TGTCTTTGATCTTC | - | 6.41 |
|
| | 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 |
| GH11I113445 | chr11 | 113316422 | 113319671 |
|
Enhancer Sequence | AAAAAAAAAA AGGAGAGAAA GAAAGAAAAG AAAGTGCTGC TTGTTCCAGC ACCTGCAGAG 60
GATGCGAGCC AGCCAGCAAA TTCACTACTC ACCTTGCATA TGAACGAACA AACACACACG 120
GGTTTGGTGG GCAACAGAGA AGGCAGGCGG AACTCTGGGG TGTGAGTGGT CCATGAAGCA 180
AGACAGACAG ACATGGGGCG GGGTGTGTAG GGACTGAATT CTGACAGGCA GTCAGCATCT 240
GGCTTCTGGC CCCTGCTCTG CCCCACATTT CCAACCATGT GACCTCAAGC AAGTGGCTTC 300
CCTCTTCTGG CCCTGGATGT CCTTTTGTAA CAAACATGTG TGGCCACATC AGAGGACACA 360
CAAGGCTTCC TCCCACCAGT CCTAAGATTC TAATCTGCCA TGATGCGATC TCCAGCCTTG 420
TCCATGTTGA GGGGCCAGTA GCTGAAGGAG GGAGCTCAGG GTGCCCAGGC CCTCCCTGCT 480
TGTCAGTCTG GGGACAACTG TCTATTGTGG TTAAAGCAGG TGTCTGAGGC CATGATGAAG 540
GTAAGATCCC ACAAAGGGAT ACTGAGGGGG CTCTAGATGG TGTCTGGCAG CAGAGAATGT 600
AGTCAGAGGA CCTTCAGGCT AGGAAGTCAT CATCACTCTG CGAGATGGAA CCACGAAACA 660
GGGAGTGAGT GAGTCACCAG AGATAATGAG CTCCGAGGCA GGAAGATGCA GGAGTCTAAT 720
GACGTTCTTT TCCTGTCCTG ATGAGATCTC TTGTCCATAG GCCAGTAGAG CACCCAAGCC 780
CAGAGCAATG GGTAAGGGGG TCTGACTTCA ACCTGGGGCA GCCGCTCCTT GGAAGGAACC 840
AGGCAGCAAC TGTGATTCCA GCATCCCAGC CCAGCCCAGA TGCACGGTGG CTGAAAACCA 900
CGCCTCAAGC TCCGGGGGAA CTCCCTGGCT ATTCTTGGAA ACACAGAGAC TCCTGGCTCC 960
CTGTCAGAGC TGCTCCCCAC TCTAAAAAGC CCAGGAGTCA CTGCTACAAT ATTTTTCCTT 1020
CTGAAGGAGG TGGCATCTCA GTAATTGCAA CGTGATGCTC TCTTGACAGC AGTATTAATC 1080
ACCTGTCTTC ATCTCAGCCC CAGCCATGAG AGAGGAACAG GAGGAAGACA GAGCCAGAGG 1140
GCCTGGTGTT GTTCACTGTC CTCATCCAAG GGCACGGGTA CAGCAGTCTA TTCTGTCTCT 1200
TCCTCAAGCT CATTGTCACT TCCGAGAGGG GACTGGGGTC AGGCCTCATT CGGGTTCCCT 1260
AGAGTGGAAA GGATTGGTAA GGAGCTGGGT AGCTCTCCTT GGCCACCTCT AAAGGAGCTG 1320
CACCACACTG GGCCTGCGAA GAGGAGACCA GGCCCACAGA CCCAGGCAGG ATGGAGGAGA 1380
TGGGAGGGGT CAGCAGGGGG CCAAATTCAA GAGTTTCTTC TCAACCCTAC CTTTAGCCTG 1440
CCTTCCTGAC CATCCTGCAC ATGCCCACCA AGTCCACCTC CCAAAGCCAT GGCTTCAGGC 1500
TCATGTCACC GCCTCGCTCA AAATATCTTC TATGACTCCC CTGAAGGGAA AAGTCCAGAT 1560
TCTTTAGCTC TCTGTCTTTG ATCTTCCCAC ATTACCTGCT GGCCCCTCCT GTGGACAGGC 1620
TAGACTGCAG CTGGCGTTGA TCTAGTCTGT GACTTTTGTA CCCCTCGCTT CCCCTCATCC 1680
TCCTTTGAAT GCTGCCATTT 1700
|
