| Tag | Content |
|---|
EnhancerAtlas ID | HS003-41252 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr7:28353920-28355340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr7:28354680-28354694 | TCTTATCTTATCCT | - | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 28354161 | 28354225 | | chr7 | 28354335 | 28354965 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I028315 | chr7 | 28355203 | 28357034 |
| Enhancer Sequence | CCCTCCTACA TTCAAAGGCT GGAAATTCAA GTATTAGAAC ATTCATTACT TTTTCCTTGG 60
AGATGGTGCT GTCTTTATCA TCCATCTTCA TCACTTGCTC CAAGTTAAAA TGGTTGATTT 120
CTTGCTGCTG ATTATAGGGC ATGAATCTTA GTCCTATGGA GCTTGAAAGC ACGATGGCTT 180
TGTGTTCTTC AGTATCTCTG AGCTTCATTT TCATTGTCTG GTCAAAACCA GGAGAGTAAC 240
ATCTGCCACA CAGATTATTG TGATATATAA TGTGAAGATA CAGACAACAC ACACAGCACA 300
GTGTCTGATG ACCAAGACAT GCCAGTATCA TAGTTCATAT ACTTTGGGGT AAGGCTTAGT 360
GAGCAGCGAC ACACTACCCC AAGGGAAAGA AAACCAGAAG GGCACTTCCT GAAGGGGAAT 420
CTTGCTCCAG GTCCCCAGTG TCTCTTTACT GAGACGCTTT ACTGAGACAG TTCTTCCCCA 480
ACTGGATCAC CGGTGTGCAA TTTGACCTTC AGAAGTATGT TGTAGAAAAG TGCTGTACGG 540
TCAGTAAATT TGGCAACTGC TGCCAATGGG CACATCAGCG TGTTGAAGGC TGTAGAAAGC 600
CTAACAGTAG AGAAAACTGT TCAACTTTGT TTAATGTAGC ATTTTTCTAA CCATATTCCA 660
GTGACAGGAA CATATTTTCC TGCCTCAAGA CTGGTATGCC TCAAAGCACT GTTTGGGAGC 720
TGCTAATCCA AGCCCTTGAA GTCAGTAGGA GATAAGGGTA TCTTATCTTA TCCTTGGTGT 780
TTAGTGTGGT CCCAGCCTAT ACAAGGTATG GAACAGACGC TGGGTGAATA AATGGCTCAA 840
TGTATATGTC AATTTCCTGA TGATTCTTGC CAAGGCAACG ACTTCCTGTG GGCACAATTC 900
ATTTGTATTG TCACCACCAA CAGGGACTAC AGCACAAATC CTTCCCACAT AAGCTGGCAT 960
TCCTACTATG TTGCCAGTTT AATGAATTTT GTTAAAAACA GACTTCTGAC CAGCCAGGGT 1020
CCTGATTTGA CAATTTTATT TTTTCGGAAA AAGTCACTAT GATGACTCTG TTTGCAGCAG 1080
TTGTCCGAAG CTGAGGTTGC CTTCTGTTAG CCGCTTCTCT TGGTTGGACC TGAGCAATGG 1140
GCAGGTGCCA GAGAACTCTG GACAAGAAGA CGCTTCCAGC CGGGTGCTGC AGAAAACTTG 1200
TTCTGCAAAA GCAGACAGGA GACACTGAAT GAAGGACTCT GTTCTCCAAC AACAGATTTC 1260
ATCATTGTGA GGTTCACATG GGGTGTGTTT TCATTTTGTT TTTCCCTACA GTTTCAATCT 1320
TCTTTCCTCC CAGAAAGGGT TCTTTTGTGT TTGACCTCGT CCCGACGCGT TGGAAAACGT 1380
CCTGCTGCAC CAGCTCTTAA TTCACCTTCC TGTGTGGACT 1420
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