| Tag | Content |
|---|
EnhancerAtlas ID | HS095-05782 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:77312780-77314220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFK | MA0496.2 | chr11:77313564-77313583 | AATTGCTGAGTCATGAATG | + | 6.35 | | NFE2L1 | MA0089.2 | chr11:77313565-77313580 | ATTGCTGAGTCATGA | - | 7.6 | | Nfe2l2 | MA0150.2 | chr11:77313567-77313582 | TGCTGAGTCATGAAT | - | 6.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 77312851 | 77312937 | | chr11 | 77312988 | 77314161 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I077601 | chr11 | 77312492 | 77315150 |
|
Enhancer Sequence | CTGACCAGTG GTGAGGCTGG AAAGCCCAAG GTAGCCTCAC TCATATGTCT GGCAGTTGTC 60
AGCTGTCATC TAAGATGCCT CAGTTCTCTT CCGTGTGGCC TTTCATCCTC CAGCAACCTA 120
GACCAGCAAA CTTACATGGT CAGGGCATTC TTCCAAGAGA GCAAAAAGTG GAAGCTGATG 180
GGTTTATTGA GATGTGAACC TAGAATTCAC ACAGCATCAC TCCTGTTACA TTCAGAATTC 240
CCATAGCCCT ACTCTGCTGC ATTCTATCAA CACAAGTTGC AAAGCCAGCT CATTTTTAAG 300
AGAGGGAAAG TAGACAACGT CTTGCTGGGA GAAGCAGCTA CCACTAAGTC ACACTGATCA 360
GAACTGCTGT GTGAGGATGA GAAGATTAGG AAGTGAAGTC GTTTGAGTTT TAGGATGGCA 420
TAAGACTGAT CAGTGGTGTT CATCTTAGAT CTAGTGGAAA ATCTTCAGTA TACCATGGCC 480
TTGAATACTG AAGTAAACTA AGTGAGGGTA ATGATTCAGT CCATTTTTAT CAATACATGC 540
CTAAAAGTCA CAGGTCATTT ATATCATCAT AGGTCATATT ACATTATATT GTAAATGTCT 600
GTGTGAGTCT TTATCTTTCT GCCCATGGTA TCTAGTACAC AGGAACTCAA TAAGTTTTTG 660
TGTAATCAAA CTGAAATGAC TAGCTGCCAA CCAGACAATT CTGTTCACCC TTAGCAGTGG 720
CAGGTTTAAC ATTCCAGGAT TTGACTGTTC AAGAATGATT CCAAAGGTCT ATGATATCAT 780
TTATAATTGC TGAGTCATGA ATGTGAATCA TGCTGTGAGG CTGGTACACT AGAAAAAACT 840
CTTAGCTATT GAGTGAGCTT AGTTCATTGC TAAATATCTT CATCTCAACA CAGCTTCATT 900
GTTCTCGGCC TATTCAAGTG TGAAATCTCA GTAGTGAAAT CTTATGAAAG GGCCACTTAA 960
TTTCCATGAA AACAGGCTAC AATGGTGCAT GTCAATAATA AAACTTCTGA AGATCTCAGG 1020
ATCTATCTCT GTGGCTAAGT AAAAGAGGCA GAGTTGTGTG CCTAAGCTTC CACTTGGAAA 1080
AACTGCTGAA AATGTCACTG TCTGAGGGAT GCTCTTAGGC TGGACTTTGA AAAGCGAAGA 1140
CACAGCTCTG TGGAGTACTG CTGGACAGGC ATCCAGCCTC CTCTTCCATT CCGCACTTGT 1200
GTGGCCAGAC TATAGACTCC TAGCCCCATG CCAGAGAAAT ACCCTGGGTG CAGAGCTGGA 1260
ACACAAATCC TAAAAAGTAG CCAACAGTTA TAATTTGTGC TTATCTCTCA TGACTACTCA 1320
CAGTCCCTTC TTAAGGGCTC TGTTGACAAG TAAAAATAGA ACCAATGATA AAGCTTTGGT 1380
CTATTGGTCC ATTTTACCTT TTCAATACAA AGTTATGCTT GTACTCAAGA GGATCTTGGG 1440
|
