| Tag | Content |
|---|
EnhancerAtlas ID | HS082-00401 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:23157900-23159350 |
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 | GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA CTGTGTGCCA GGCAGCCTGT 60
GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC CCTTACAAGT CAGTCTACTA 120
TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA GCCTGAGTGG TTTGCCTAAG 180
GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT CAGAGCCTTA ACACCATGCC 240
ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG AGGGCCAAAA 300
TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG GGCTTCCTCA 360
GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT 420
GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA GCTATCCACC 480
CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC CCACATAAAC 540
CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG GCTTCCCCAG 600
GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG AGGACCTTCG 660
AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA AAGTAGGGAC 720
AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC ACGTCATCAG 780
AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG GGTGAGTCAT 840
GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT GCCACCTCTC 900
AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT TGCCAATGCT 960
ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC ATTCATCCTT 1020
TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC CAGAGAGGTT 1080
AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA CCCCTAGTGA 1140
TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC TGGGTGGTTG 1200
CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC TCCCTGACCA 1260
CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC ATTTATCAGA 1320
GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT GAGGGTTCAG 1380
CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT GACTACAGCA 1440
CCTGTACAAA 1450
|
