| Tag | Content |
|---|
EnhancerAtlas ID | HS095-10929 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:4734020-4735160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr16:4734473-4734488 | GGGTCACCCTGCCCC | + | 6.83 | | TFAP2A | MA0003.3 | chr16:4734124-4734135 | AGCCTCAGGCA | + | 6.32 |
|
| | 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 |
| GH16I004684 | chr16 | 4734821 | 4734970 |
|
Enhancer Sequence | CAGCAGAGGC TGTCCATTGG AGCCTGGTTC TCTCCCTGGC TCTCAGCCAT GCCCCTGCTA 60
TTGACCGTGA AGCAGGATGC GGGCCAGGGC CATGGCCACA AAGCAGCCTC AGGCAGGGCC 120
TGGCTCTTGG GAGCGGAACC TGCACCAAAG CCCCTTCCCT CCCTGGGGCC ACATTGGCCA 180
CAGGAGGTGA GAGACGCGAG AGAGGCTGCC TGTGAGAGGA TGGGGTCCTT TTCCCTCTGC 240
CTGCTGCTCA CGCCAGGAGG GCAGATCCGG CCCCACTGGG ATCACCACAT GTTCCCCCAC 300
TCCTGGTCCT ATCGTGGGCC CACAGGCCCC ATGCTGGGTG CCACGTGCGC TCCTGGCAGT 360
GCCTGAGAGC TGCAGACAGA GCAGGAGCAG GTACCACACG CTGTGCTGGG TAGCGGGGGC 420
CCTGGGCCAC AGAGCGCAGG GGCAGTGTCT TCTGGGTCAC CCTGCCCCGG GCCTGACAGA 480
GGCCACCTGA TGCAGCAGCA CATCCCAGGC CAGGCACAGA GGACGGCGGG GGCGCCAGGC 540
GCCAGCGGGG AACAGCAAGG CAGCAAGGCT GGGACAGAGG GTTGCTCTTC TCACCTTTCC 600
CGGAGGCTCG GGCCCCAGAC CCCATCAGCC AAGCACCTTC GTGCTCTGCT CTGCTGGGAT 660
AAGATCCTCA GTTTCGAATC CTAAGCTCTA AAGACCGGGA GGGAATGGGG GCTCTCAGAC 720
TAGTGTCTCA GCACCTGCCA CGAGGCTGTC TGCGGCTCTG GAACTGCGAT AAACAGCCAC 780
GGTGCTTTCA GACATGACCC CAGAGCCACT GCTTAGGGAG TGTGGCTCTT CCCTCGCGGC 840
TGCCAGGCTT CACCCGCTTC CTGGCCCCAG GGCCCACCAT TGCTCAATCC TCCTGAGTCA 900
CCTGGTGACC TGGGCCTGAC ATTGGGTGGT TGTGACGTGC TTTAGTTGGA AAGGGGCTCT 960
TGTGCCCCCG GACTCTGGCT GAGCAGTGGC CTGTGCTCAT GGGCTGGGCG TGACAGGTCG 1020
CAGGTGCAGG AGCAGGCACT GCCTCTGGTG CCCTGATGAC CACAGCGGCC TGCCCCGAAC 1080
AACTCACAGC AGAAGGTGTG TTTAGGACCA GCTTACCTTA AAGTGACACA GAATTCGAGT 1140
|
