| Tag | Content |
|---|
EnhancerAtlas ID | HS089-07243 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr2:33598490-33599940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:33599539-33599549 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:33599539-33599549 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:33599539-33599549 | AATGGAAAAT | - | 6.02 | | TBX20 | MA0689.1 | chr2:33599143-33599154 | GAGGTGTGAAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGCCTATTG AATAAAAGAA TAAAGCACAA AGGCATGATG TGAATAGGCA CTTAGTGAGG 60
ATCTGTTGAG TCAAAGCAAT GTCAGTATGT ATCCAACTTC CTTTGAGAAA GGTAGACTGT 120
GCTATAGGGG AATAGAAGAT ATTTGTCAGT TATTCATACT CCTTTAAATA ATGCTAGGAA 180
GAATTATCAT TACTGTATAT AAATTATATA CAGCTTGTGG TTTATAAGAA GAGATAAGTA 240
AATGATCTGA AATGAAATCT AAATTATTTA TAACTTACCT GTTTTCAGTT TTAGTTAAAT 300
TACTTACATG TTCTTTATTT TATTATTTAT TGAATGCCTA CTATGTACTA GGCAAACAAT 360
TCTGGAACAG GTGTAAAGTT GTATTTAATG AAATGCATAA TTAGTATAAT TTATTCCTAA 420
ATATTATGTA TTTTAAATCT GCAAATGATA CTTTAATAAA TTCACCATTT GCTGTGACAG 480
AAAATTTTTC AATCCTTCCT AATATCTAAC CTACCCAAGT ATTCATATCA TTTTGCAAAA 540
GTAAAGAATT TGGAATGTCT TCAAACAATT CGGCTAGTGA TTTCTTCCAT ATCTGTGCAT 600
GGCTCTTAGA CGCTCCCAAA GATCTCAGGG CAAGAAGTTT CGTAATGCCC TTGGAGGTGT 660
GAAGGAAGAC AGGGATTTGA CTCATGGACT AAACTTGAAA AAATATTGTA ACTGGGCCAT 720
AGTTGCAAAA GGCCTGTCAG CAGTCACGGT TTAAAGGCTT TTCCAAGAAA TATGTTTCCA 780
AAGAATGTTA ATAATCACTT TGGAACACCC TACTTGTGAA ACAATGAGTG GTCACTGCCT 840
TTGGTTTAGG CAATCCAGGG ATCTCTTTCT GCTTTTGGTC CTGGCTCTGT GACATTGCAC 900
TGGGCACATT ACTTCAACCT CCTTTATCCA AAGTTGAGAC CTCTTCGTGA GGTTATGATA 960
ATTAATACAA TCACTATGAA AGCATTTATC ATTTCAATCA TAGATCCTGA ACATTATAAT 1020
TAAAGAAACA ATAACCGCTA GTCACTTACA ATGGAAAATT AAAATCAAAC TAGAAAGATA 1080
CAAAAGGAAA TCGAGTGGCC GTCATGCGGG CACAGAGAAT ATCTATAAAA CAGGCAAGCG 1140
TTCCAGTTCT GTGGGACTGA ACTCTTGGTA TCCATGGAAC TAGATTGAAT GGATGTTATA 1200
TGAAATGGCC AGTAAGCCAG TTATGTTGTT CCTCATTGAA AGGACTCTTG GCCCGGCACA 1260
GTGGCTCACG CCTGTAACCT CAGCACTTGG GAGGCCAAGG TGGGCAGATT CTGAGGTCAG 1320
GAGTTCGAGA CCAGCCTGGC CAATATGGTG AAACCTCATC TCTACTAAAA ATACAAAAAT 1380
TACCTGGGTG TGGTGGCGTG TGCCTCTAGT CCCAGCTACT CTGGAGGCTG AGGCAGAAGA 1440
ATCGCTTGAA 1450
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