| Tag | Content |
|---|
EnhancerAtlas ID | HS042-11083 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:104900380-104902030 |
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: 2 | Chromosome | Start | End |
| chr12 | 104901200 | 104901600 | | chr12 | 104901600 | 104901872 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH12I104506 | chr12 | 104900741 | 104900890 | | GH12I104507 | chr12 | 104901021 | 104901170 | | GH12I104508 | chr12 | 104901344 | 104902654 |
|
Enhancer Sequence | CTAGCTGTGC TGTGCCACTT TGAGAAACCT AGTCCAGGTG CTAAATTTAC AGTGATCACC 60
TTGGGATTCT GGTGTCCGAC AGAGATGGAA ACTTCGCAGG AAATGTTCCC CAGGCGGGAG 120
GGCTAAGAGG ACACAGTAAC TCTTGAGAGT TGCTCCGACA GACCTTTTAT TTTGGCAAGG 180
GCTTGTGCTT TCTTTGCCAA GCCATCATTC GTTACTTGGC TAGAGGAGGG ACCACAGGGA 240
GGGGAGAGGG GACATATACA GCTGGCTGTC AGAACAGTCG ACCTCTAAAT GGGATAACCT 300
CAGAGCCAGG CATAAGCAAT CTGGAAACAA GGAGGGGAGG TGATGGAAGG TGGGAGCAGA 360
GGCAGGTGCT GGAGACATTG CTGCAGACTT CCTGGAAGGG GTTGCCAAGC CGGGAAGATT 420
CAGAGGGGAA GAGCACAGCT GGGGAGAGAG CCCCTGCTGG CTCCAGGTGC TGGTCCCAGA 480
AGGCATCTTT GGAGGGAAGG GTCTGAGCTG TGACGGTTCA GTGCAGGGAC AGGTGGGGTA 540
AGCTCAGGTG TGCCGGGCTC CCTGTGCGTG TTGCAGAGCT CCCGGGGAGG GCAAGGATGT 600
GAAGTGCGAG CAGATGGTCT CCGTCACTGC CAACCTAAAT CAATGACTGG AGAGGGCGAA 660
TGCTGCCAAT TAGCAGGATA TCCAGAGCTC TTTCTCCCAG CCCAGTGGCC CCACCTGGGA 720
GCCAGGCAGC ATGCTTTGCC TCCTGCTGAG ACAGATCCTG CTTTTGCTGC TTCCTTGAGA 780
GAAGTTTTAA CACATGAAAA TGGCTAAGAG CAAAGGCTTT GGCACCGCTG CCTGCTTTCA 840
GATTGCTGCT TTTGCTAGCC ATGTCATCTT GATCCTGTTT CTTCCCTTCT CTGGGCCTTG 900
GTTTCCCCAT TTGTAAAATG GTAATGGTGG CAATAGTACT CATCAGTTAT TGCCACCACA 960
ATGCTGCCCA GCAAACTACC TCAGTAGCAC ACAGTAGTAA GTGTTTGTTG TTCACACATC 1020
TGGGCTGGCC AGAGGGCTTT GCTGGTCTTG GCTGGCCTTG CTCATGTCTG GATGGCTTTG 1080
GCTGAGGGGA ATGACTGAGA TGATTTGTCT CAGCTTCCTG TATCTCTCTC ATCCTCCTCT 1140
AGTGGTGTAG CCCAGGCAAA TTCTCATGGA TCTGGCAAAG GTACAAGAGC CAGTGAGCCA 1200
CTCATGTAAC TGCTTTTAAG TTCTTTTCTC ACCCGCCCCC CACCATGTTT GCTGCCATCC 1260
CATTGGCCAC AGCAAGTCAC ATGGCCGAGC CCAGCATCAA GGCTCCTGGC AGACTGCACT 1320
TCCCAGGATG GCACTGCAGA GTCACAGTGC CAAGGTGTAT GGAATTGGGG TGTTTTTTGC 1380
AATCTACCAT GAGTACTAAC CTCACAGTTT CGTATGCAAG CAAATCCTCA TCCACTTACC 1440
AGTCTTAGGA CAGAGGATCC TCACTGGTCT CCTCGACCTT GAGACACCCA GATTAGGAAT 1500
TCTTTTCTCC TCTGACTTCT TGTAGTTCCC TCCATATACT GTTCTATTAC CCCCGTCCAT 1560
GACACCTTTG TACTGCTGTT CCTTCTGCCT GTAATGCCTA CCCCTTGGCT TACCCATCTG 1620
ATCAACTCAG CTCTGGGGTC AGACTGTTTG 1650
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