| Tag | Content |
|---|
EnhancerAtlas ID | HS136-01441 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr1:182139460-182140950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr1:182140501-182140513 | CAAGATGGCGGC | + | 7.22 |
| | | 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 |
| GH01I182170 | chr1 | 182139736 | 182140935 |
| Enhancer Sequence | AATAATTCAC ATTCAAAACA AAATGATACC TGTCTATGGC AGCTCCAGAA CACTCCCTAA 60
TGTGCCATAG ATGTTTAAGA AACTCATTCC ACACACTTCC TTTAAGGCAT TCTCAGGTTT 120
CCTAAGGCAA GCTAGCTTCT ACCTCCCTTT TCTAAAGATG TGCCTAATGA TCTAAAAGGA 180
GGTGGGCCCC TCTATGCTAC CTCATACAGG TACTTGGGCA ATAACAAGAT TGTGGTTTCC 240
AGAATAAATA ATGGGCACTG CCACCATCGG AGTCCATAGG ATGCTGTATG AGTGCCAAAC 300
AGTTCAGGCT GGCATCTCTG TTAGTTTCAA ATGATAAAAT GCTAGGCTAT AACAATGTTT 360
AAAGATTATC TCTTCCAATT CCTTCAATAC ATTGTCCCAA GTCACCTGGG ACACCGTGAA 420
TGGCCTTCCT TCCCAAGCTC ATCTCCTCCA AACATATCCA GCTCCTCTTT TCCATTTTAT 480
CTATTACGAT AAACAGAGTG TCGTTACCAC AGAGTTCAGC AATTCATTTC CCTCTGTTTT 540
TTCCATGTGT CTATTATTCT ATGTTTCCAT ATAGATGGCA GCATCCCCCT TTGGCCTTCC 600
CCTCCTTCTC TGGCATGTAT TCTAACTGCT TGTCGACGGG TGCCAGGAAG TCTCAACCTT 660
ATGTAGTCTT TCAGACAGAA GGAGAACCTA GCTGACAGCA TTGTCTCCTA ATTTTCTCGT 720
AAGACGAAGT ACAGCTAGAA AGGAGAAGCA TAAGTTTCAG AAGAGGAATC TGACCACGTG 780
GAGGAGACTT TGCTGTATTT TCTAAGAAAT CTTTGTGATT AACCAAATAT GTTGGTTATG 840
ACACTTTCAG CTGCCTGAAA CAGAAAACTC CCACTCACAC AGCTTGAAAA ATGCAAACAA 900
ATGTATTGTC TCACATACTT AAAGTCCAGA GATGGCTTGG GTTTCAGGAA AGATACGGTT 960
CAGTGCTATT CAGTAATGTC ATCAGGGACA GAGGTTATTT CTGTCCTTCC AGTCTGCTGT 1020
CCTCAGCATG GGTTCATTCA ACAAGATGGC GGCCACTGGA TATCAGCTGG CCACACACTT 1080
CCTGTTCATA TCCAGTAGGA AAGAATGAAT GGAAGTAACC TCTGCCCAAA GGCCCCTCCT 1140
TTAGTCTGAT TGGGCCAAAT TAAGTAATAC ATTCATCATT GGCCTAATAA CAGTTGCCAG 1200
AAGGATGTCA TGTGCTAACT GGTATAGATC AAGGCTTTTC AATAGCAGTA ACACTGACAT 1260
TTTGGACTGG ATTCTTCCTG TTGTGGGGGC TGTTCTGTGT ACTATAGAAT GTTTAGCAGC 1320
ATCCCTAGGC TTTATAGTCC CTCAGCACCA CCTGTCATGA GAATTAAAAA TGTCTCCTGA 1380
CATTGCCAAA TGTCCCCTGG AAGACAGGAA AAATCACCCC AGGGCTGAGA ACCACTGGTA 1440
TAGACTAATC AGGTTACTTA TGGCCTCTGC ACCTTAGTTT TCTAAGATAG 1490
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