| Tag | Content |
|---|
EnhancerAtlas ID | HS081-00236 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:23158050-23159440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
|
| | 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 |
| GH01I022824 | chr1 | 23151232 | 23159621 |
|
Enhancer Sequence | GGCTCAAGGA GCCTGAGTGG TTTGCCTAAG GTCAAGCAGA GCAGGGCAGG AATCCAGGGC 60
TTTCCAAATT CAGAGCCTTA ACACCATGCC ACACTGTGCT GGCAGAGATA GCAAGAGTTG 120
TTGGAGATGA TTATAAGGGG AGGGCCAAAA TGATCGTGGG AATCCAATCC CCGTGGCAGT 180
AGGTGGGAGA TGCTGACCTG GGCTTCCTCA GAAAGGTGTG AAATGTTGAC ACCCTCCCCT 240
TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT GTTAGGCTGG GCTGGAAACA GAGGGCTGAC 300
CATCATGGGT TCCAGAGGGA GCTATCCACC CCCCTACCTA GCCAGAGGCA GCCAGGATTC 360
CATTAACCTG ATTCTCTGCC CCACATAAAC CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA 420
CTGGGGAGAG GAAGAATTGG GCTTCCCCAG GCCCCAAATG GAGCAGCCAG TGGTGCTAGT 480
TTCCTCTCTT GCAGTCCAGG AGGACCTTCG AGGCCCCTGG CTGTTTGAGC GGGGAATAGG 540
GAGAGCGATG GAGAGCCAGA AAGTAGGGAC AAGAGACTCC AGGCTGGGGT GCAACAGCAG 600
GAATAGCAGG AACAGGGTGC ACGTCATCAG AACAATGGGT CCTGAGTCAC TCTGTGCCTG 660
CCCAGCCCTG CATGGCCCTG GGTGAGTCAT GTCACTTCTC TGAGCTGTGG GTTCTTCCTC 720
AATAGTAAGG GCAAACCAAT GCCACCTCTC AGTGTTGCTG GGCTGATTCA CAATACCGGG 780
CCTCAAGAAA TGGTGGCTGT TGCCAATGCT ATAATTTTAC AATCTTGACC CCATGTATCC 840
CTTCTCAGCT TGCAAGCCAC ATTCATCCTT TTTCTCCTTG GAGCCTCACA ATACTTCTGC 900
AAGGTGTCCA GGATTCTTAC CAGAGAGGTT AAGGGACTTG TTCAGAATCA CACAGCTTCT 960
AACCCTTGGC CTGGGATGCA CCCCTAGTGA TTGTCATGGA GTGGGCCATC CCAGCCAGGC 1020
TACGCCACTC TTCTTCAGTC TGGGTGGTTG CTATTCCTCT GCCATGATTC ACGTCAGATG 1080
CCTCTTCCTC CAGGAATCCC TCCCTGACCA CACAAGAGCC TGGTTAGTAC AACTCTCTGC 1140
TTTCCCACAA CCTTTGAGAC ATTTATCAGA GTGTTTATCA GCAGTCATCA CAACCGTTAG 1200
GTGCTCCCAC CTAAGACTTT GAGGGTTCAG CCAATACTTT ATAATAGAAG AAGAGGGGGT 1260
ACAATAAATA TTTTGTTAAT GACTACAGCA CCTGTACAAA GGGACAGATA GGTGTCCACA 1320
GACTCACATG TATAAGTAAC AGTCATGCAT GCACAGCCAT GCACATGTGG CTTAGTGAAT 1380
ACACATGTAT 1390
|
