| Tag | Content |
|---|
EnhancerAtlas ID | HS095-17025 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:132426620-132428190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | + | 6.37 | | TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | - | 6.5 |
|
| | 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 |
| GH02I131667 | chr2 | 132425552 | 132428164 |
|
Enhancer Sequence | ATGACCTCTG CTGGGCCACC CAGCAGGCTC TCAGCAGATG GTAACTATTT TAGGCTTGCT 60
CAGGCATGTC TTGTGACCTT CTCAGGGTCA CACAGATGGA AAACAGGAAC TTAAAAAATC 120
CTTATAAACT TACAGAGATA GTTACAAAAA TAGTTATGAG AGCAGAACAA AGAAATATTG 180
GCCTGGGAAA GAATCTCAAA GGGGGAAGCT GATAAGAACT TGTTTTTCTC ATCCCTGTTC 240
CTGGAGTCCA TTCCTTCTGG GCTCTTCCTG GCCTTGTATA TAAAGTTATC TTAATTCTAG 300
CACGGCCTTG GAGTGAGTCA GCCTGGAACA GGCAGGAACT TAGGTTTTTC TCTTTTTAAT 360
TTCTGCTTTA GTAGGCCAGG GTTCTGATTT TCACTGCTGA GAAAGTAAAG TGTGTTCAGG 420
CTGCCCATGG TTCTGGGCCC CCCCGGGTCT CTGAGGAGGG CTGTCCCCTC CATCACAGAG 480
AATATCAGGA CACTAGCTTG TTCTAGTTAT ACTTACACAC TCCTCTCATG TTGTCTATGG 540
AGTGGTGGAT GCTGCAGGGA GGGTGACATC CTAGTTAGTC CTAAGAGCCA GACTGCCTGA 600
AGCTCACTAT AACAAGTCCT GCCTTGGGGA AGAAGGAAGT GTGTCTCTGT GAACCTCCCA 660
CCTGGGCCGA AGGGAGGCCA CTCTCTCTGC TGCCTCTCCC CAACCTTGGC CTTCTGTGCT 720
CCTAGTGAAC CTCTCACCCC CTGCCTACAG GCCTCGAATC TCAAGACCAT GATGACCTCT 780
GGTCACCCCT GAATCCAGAG CTTTCCTTTT ACAAAGGGGA AACTGAGACC TGGAGCAGGG 840
CTGATGTTCA GCCAGCGCAC AACGGAATGG CCGAATTGGT GGTAAAATAC TGAAATAGTT 900
CCAGTGTGGA TGGAAAGGGG CTGCTGCCCT AAGCATCTCT ACTGCCCACC TCATCCCTTC 960
CTCCAGGACC CTGGGTCAGC ACCAGGAGCA TCAAAGTGGC CAGGATTGGC CGGAGCCCAT 1020
GCTAATGGCT CTGCCAGCCC TTCTCCCCAC CAGAGAGGGC AGGGGGATTC AGGCCATCTA 1080
GAGGTAGCAT TGTGACCGTA TCTGCAGTAG TCAATCCTTG TGTGCCACGG TCCCTGACTT 1140
TGTTAATAAG GGCACCAGCC TACATCCCTC TGGTACTCAG TGATAAGCAT CTAAAATCTT 1200
CTTAAAGAAA AAATTTAAAA AGCTTTCAAA ATATATGACT TAACATATGA GGCTGCATAA 1260
ACATCTCTAG TAGTTGTCCA ACTGGTGCTT CTGGTTCTGC CTCCCCAGAA AGTGGATGAC 1320
CTGGGCCACC CTCCACCACT GCCCTGTAAG GCCATGGGAC ACACAGCCCA TCAGTTCTCT 1380
TCATGTGGTC ATCCCCTGTT AGATGGGAGA AAATACACCT GCCTCATTTT TGTACCTTCT 1440
GTGTGAACAT TCCACGACAG AACTTCACTA AATGTGTGAT GAAGAACTGA ATGAATGAAT 1500
GAATATGAGA GAAAATGAAT AAATGGCTCA GATCCTGGGC TGGAAGTCTG TGTATGAGGA 1560
TGGTGGGTAA 1570
|
