| Tag | Content |
|---|
EnhancerAtlas ID | HS108-33605 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr6:3171480-3172640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr6:3171717-3171732 | AAACGCACCAATCAG | + | 6.73 |
| | | 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 |
| GH06I003171 | chr6 | 3171719 | 3173319 |
| Enhancer Sequence | GGAGAACCTT TATGTCTAGC CCAGGGATTG CAAATACACC AATCGGCACT CTGTATCTAG 60
CCCAAGGTTT GTAAACACAC CAATCAGCAC CCTGTGTCTA GCTCACGGTT TGTGAATGCA 120
CCAATCAACA CTGTATCTAG CTACTCTGGT GGGGCCTTGG AGAACCTTTG TGTCGACACT 180
CTGTATCTAG TTAATCTGGT GGGGACGTGG AGAACCTTTG TCTAGCTCAG GGATTGTAAA 240
CGCACCAATC AGCACCCTGT CAAAACAGAC CACTAGGCTC TACCAATCAG CAGGATGTGG 300
GTGGGGCCAG ATAAGAGAAT AAAAGCAGGC TGCCTGAGCC AGCAGTGGTA ACCCACGACA 360
GTTCTCTTCC ACGCCGTGGA AGCTTTATTT TTTCGCTCTT TGGGTCCACA CTGTTTTTAT 420
TGAGCTGTAA CACCATGAAG GTTTGTAGCT TCACTTAAGC CAGCGTAGAC CATGAGCCCC 480
CTGGGAGGAA CAAACAACTC TGGATGCGCT GCCTTAAAGA GTTCTTAACA CTCACTGTGA 540
AGGTCTGCAG CTTCACTCCT GAGCTAGTGA GACGACGAAC ACATCCGTAA CAGCAGAAAC 600
AAACTCTGGA TGCACCACCT TAAGAGCTGT ACCACTCACT TCGAGGGTCT GTGGCTTCAT 660
TCTTGAAGTC AGTGAGACCA AGAATCCACC AATTCCAGAC ACATAGATCC TATTGCTCTA 720
GGCAACGCTT ATGCTGATGA GGTGGCTAGA CAAGCAGCTA GCATTCCAAC TTCTGTCTGT 780
CATGGCCAGT TTTTCCCCCT ACACGTTGGT CACTCCCACT TACTCCCCCG CTGAAACTTC 840
CACCATATCA ATCTCTTCCC ACACAAGGCA AATGGTTCTT AGGCCAAGGA AAATATCTCC 900
TTCCAGCCTT ACAGGCCCAT TCTATTCTGT CATCATTTCA TAACCTTCCA TGTAGGTTAC 960
AAGCCGCTAG CCCGTCTCTC AGAACCTCTC GTTTCCTTTC CATCATGGAA ATCTATCCTC 1020
AAGGAAATAA CTTCTCAGTG TTCTATCTGC TATTCTACTC AGGGATTGTT CAGGCCCCCT 1080
CCCTTCCCTA CACATCAAGC TCGGGGATTT GCCCCTGCCC AGGACTGGCA AATTGACTTT 1140
ACTCACATAC CCTGAGTCAG 1160
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