| Tag | Content |
|---|
EnhancerAtlas ID | HS034-07471 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr12:104900390-104901860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LBX2 | MA0699.1 | chr12:104901044-104901054 | GCCAATTAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09142 | chr12:104901343-104902654 | CD14 | | SE_25350 | chr12:104900836-104902569 | DND41 | | SE_59750 | chr12:104849529-104923220 | Ly4 | | SE_62327 | chr12:104849575-104918276 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH12I104506 | chr12 | 104900741 | 104900890 | | GH12I104507 | chr12 | 104901021 | 104901170 | | GH12I104508 | chr12 | 104901344 | 104902654 |
|
Enhancer Sequence | TGTGCCACTT TGAGAAACCT AGTCCAGGTG CTAAATTTAC AGTGATCACC TTGGGATTCT 60
GGTGTCCGAC AGAGATGGAA ACTTCGCAGG AAATGTTCCC CAGGCGGGAG GGCTAAGAGG 120
ACACAGTAAC TCTTGAGAGT TGCTCCGACA GACCTTTTAT TTTGGCAAGG GCTTGTGCTT 180
TCTTTGCCAA GCCATCATTC GTTACTTGGC TAGAGGAGGG ACCACAGGGA GGGGAGAGGG 240
GACATATACA GCTGGCTGTC AGAACAGTCG ACCTCTAAAT GGGATAACCT CAGAGCCAGG 300
CATAAGCAAT CTGGAAACAA GGAGGGGAGG TGATGGAAGG TGGGAGCAGA GGCAGGTGCT 360
GGAGACATTG CTGCAGACTT CCTGGAAGGG GTTGCCAAGC CGGGAAGATT CAGAGGGGAA 420
GAGCACAGCT GGGGAGAGAG CCCCTGCTGG CTCCAGGTGC TGGTCCCAGA AGGCATCTTT 480
GGAGGGAAGG GTCTGAGCTG TGACGGTTCA GTGCAGGGAC AGGTGGGGTA AGCTCAGGTG 540
TGCCGGGCTC CCTGTGCGTG TTGCAGAGCT CCCGGGGAGG GCAAGGATGT GAAGTGCGAG 600
CAGATGGTCT CCGTCACTGC CAACCTAAAT CAATGACTGG AGAGGGCGAA TGCTGCCAAT 660
TAGCAGGATA TCCAGAGCTC TTTCTCCCAG CCCAGTGGCC CCACCTGGGA GCCAGGCAGC 720
ATGCTTTGCC TCCTGCTGAG ACAGATCCTG CTTTTGCTGC TTCCTTGAGA GAAGTTTTAA 780
CACATGAAAA TGGCTAAGAG CAAAGGCTTT GGCACCGCTG CCTGCTTTCA GATTGCTGCT 840
TTTGCTAGCC ATGTCATCTT GATCCTGTTT CTTCCCTTCT CTGGGCCTTG GTTTCCCCAT 900
TTGTAAAATG GTAATGGTGG CAATAGTACT CATCAGTTAT TGCCACCACA ATGCTGCCCA 960
GCAAACTACC TCAGTAGCAC ACAGTAGTAA GTGTTTGTTG TTCACACATC TGGGCTGGCC 1020
AGAGGGCTTT GCTGGTCTTG GCTGGCCTTG CTCATGTCTG GATGGCTTTG GCTGAGGGGA 1080
ATGACTGAGA TGATTTGTCT CAGCTTCCTG TATCTCTCTC ATCCTCCTCT AGTGGTGTAG 1140
CCCAGGCAAA TTCTCATGGA TCTGGCAAAG GTACAAGAGC CAGTGAGCCA CTCATGTAAC 1200
TGCTTTTAAG TTCTTTTCTC ACCCGCCCCC CACCATGTTT GCTGCCATCC CATTGGCCAC 1260
AGCAAGTCAC ATGGCCGAGC CCAGCATCAA GGCTCCTGGC AGACTGCACT TCCCAGGATG 1320
GCACTGCAGA GTCACAGTGC CAAGGTGTAT GGAATTGGGG TGTTTTTTGC AATCTACCAT 1380
GAGTACTAAC CTCACAGTTT CGTATGCAAG CAAATCCTCA TCCACTTACC AGTCTTAGGA 1440
CAGAGGATCC TCACTGGTCT CCTCGACCTT 1470
|
