| Tag | Content |
|---|
EnhancerAtlas ID | HS095-24255 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:80286070-80287300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr5:80286989-80287000 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr5:80286989-80287000 | GGTGACTCATG | + | 6.02 | | RREB1 | MA0073.1 | chr5:80287119-80287139 | AGTGTGTGTGTGTGTTGGGG | - | 6.63 | | RREB1 | MA0073.1 | chr5:80287121-80287141 | TGTGTGTGTGTGTTGGGGGG | - | 6.69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 80286128 | 80287179 | | chr5 | 80286375 | 80287263 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I080989 | chr5 | 80285676 | 80287424 |
|
Enhancer Sequence | TGGAGCATCA TTGATTAAAC TGCACAAAGG CACCAATGTG TTGTTTAGTG GTGGCTTGAT 60
TTCCACGTTC TGTAGGAGGT AGGTGAGCTT CCCTCGTGCC CAATTTCATG TCCAACCCAG 120
AGCCAATACT TGGAATCCTG AGAATTTTCC AAATACTCTT GTCATCCTCT TGCCAGTGAA 180
AGGAGTCGGG AGGGGGCTCC AGGAAGAAGT CGTCTAGACC CCCATTGCTA AGCCAAAAAA 240
TTTCTGCTGT TAGGGCTTCC TATCTGCCGG GGGCATTTTC CCTTCTCTAG CTGGCTTCTG 300
TTAGGAGCTC TTTGTGGCAG GAGCCCTGTT ATGTTGAGCA GGGCTGTCGG TCCACACCTT 360
TGCTGCCTCA CCCCAGTGCC CCACTGGGCT CCTGTTTGGT GTTGTCCTTT TGTACTTCCA 420
GGCTAGGTTT TTCCTTCCCA TGGGTTGAAT TGCTGGCTGG CTGGCGTCTT TCACATTCTT 480
GTGGTTTCTA AACTCCAGTG GGAATTCCTT GGTGTAAATC TGGGAATGAG CACAGGTAAG 540
GACAGTGACT TCAAATGTCC ATTGTACACT AGAAGTGCTG ACTGTTCTAG TACATGAAGG 600
TTCACAAAAG GTGAGCTGCA TAGCTCAGGT TAGTGATAGT GCTTTTGTGG GTCATAGGAG 660
TTTGTCAGTT TGTAGGTCAT AGGAGTTTGT CAATTAGACT AGAGCAGGAA AGTTATTTAC 720
CTTGAGAAAT GGCATAATCT CATTTTTCAT ATCACTGTAG ATGTCTGGGA CCCATTATTT 780
TTGTCAGCAC TTCTTAATTT TATAAGTTCA CTGACAGAAT ATCTGAACTT CAGGTACCTT 840
AGAGCCAGGC CTCTCAAACC TTACAAAGAT CTGCAAATCC CCTGGAGGCC TTGTAAAATG 900
CAAACTTGGG GCCAGGTGTG GTGACTCATG TCTGTAATCC CAGCACTTTG TAATGCCAGC 960
AATTTGGGAG GCCAAGGCAG GCAGATTGCT TAAGCCCAGG AGGTTGAGAC CAGCCTGGGC 1020
AACATGGTGA AACTGCATCT CTACAGAAAA GTGTGTGTGT GTGTTGGGGG GCCTGAGGTG 1080
GGAGGATCAT TTGAGCCCAG GCGGTGGATG TTGCAGTGAG CTGAGATGGT GCCACTGCAC 1140
TCCAACCTAA GTGACAGATG AGACCTTGTC TTTCAATAAA TAAATAAATA GCAGAATCTC 1200
AGGCAGGACC TGAGAGTCTG CATTGCTAAC 1230
|
