| Tag | Content |
|---|
EnhancerAtlas ID | HS080-20920 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr2:233830400-233831800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr2:233831564-233831577 | GTGGGGGGGGAGG | - | 6.87 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 233830646 | 233831200 | | chr2 | 233830786 | 233831223 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I232965 | chr2 | 233830441 | 233831684 |
| Enhancer Sequence | TTGTCTAGAA AATGTCTCCA CAGCAGGTGT ATCATGACTT ATCTCGCCAT GGAGATCCAG 60
CTCAGAGAAT GTAATAGCGA CATGTGGCAC AGTGGAGCTG GCGGTTCCTG CTTTGGAGGC 120
AGTCAACATC AATGTGCTCA CCAAAACCAC TGTGCTTACT AAGCCACCAA GACAGAAGGG 180
GGCACAGGTT CATGGGCAAG CTGGACTTGG TGTACAAACA GGAAGGGGCT CATTTCTTCC 240
TCCAGATTCC CCACTTCACC CTGCTCTGTA GGTTGGCACC ACCTGCATGG GTCTTGTATG 300
AAACCTCAGG CAGGCCACAT GCAAAGCTTT GCTGGCTACT TGGAAGTTAT AAGCAAATGG 360
TCTCTTTCGC TGGGTATTAA AGAGAGCAGC CCAAAGCGAT TTCCTGACTG TCTGCTTCTC 420
CCTCTCCAGG TGCAGACCCT GCCACAGCCA AAGCCCCTAC CTCTTGCTCC ATATTCTCCC 480
CACCCCCCAG CTGCTGTTTG GGCTCTCAGA GTGGGGCCCT GTGGGGGTCC TTAGACATGC 540
CTCCCGGGAG GTCTCTGACC ACAATTCCTT GGCATGTGCA AAGCTCTTAA GCCTCGACTC 600
CAGCAGGAAG TGCTCTTGGG CAGACTCCTT TTCAAATCAG TTCACAGCTG GCTCTCTTCC 660
TGGAGACCCA CACTTAGCTC TGAGAAATCA TGCCTCTCTG CCTTGCCTTC GGTGTAAATG 720
CTTCCCCAAT CCCTGCTCAG CCTTGGCCCT CCTCCCCTTG CAGGCTGCTT CAGCCAGTTC 780
AGCGCTAGAT GTTTCCGGGT GTGAACAAGG TGCCTGTTCC CCAGATTCCA GAGATTTCCA 840
AGTAGATCCA TTGAAGCCCT CCTCATTTAA CTTAAGGGAA AAGGCTCCCA TGGGGAAGGG 900
TAGGAAACTC ACAGCACCCT GACAACTCCC CCAAACAAAA CCCAGTAGCC AGCCCCGTCA 960
CTCCCCCTTT CATCTAGTGT TAAAATGCAG AAATATTTGT GTTAAAACAT TTTTATGTAC 1020
CAATTGGCAG AGAGCCACTG TCCTGAGACT CCTTCTCTCT TTACTACCAG GGCCCTTCCT 1080
TGGCCCCTTG GACTCTTGCT CTGGCTTTGG GTCCGGGTTG TCAGTTACTT TTACTCTCAC 1140
TTCTGTTGAT ACCCTCCAGT GAGGGTGGGG GGGGAGGCGG GTGAGGAGCT AAGGTGGCTT 1200
CACTGTTTCT GTTGTGTCCC AGGTAGATGG TCAGATATTT ACAGTGTTGT TCTTGGCTCT 1260
TGGGGCTTAA GCCACATCAG AGACAGCAGG AAACAATTGT CCATGGCTAT AGTTTGTATT 1320
TTTGTCCCCA CCCAAATCTC ATGTTAAATG TAATCCCCAA TGCCTGAGGT GGGGCCTGGT 1380
GGGAGGTGTT TGGATCATAG 1400
|
| |
|
|
|
