| Tag | Content |
|---|
EnhancerAtlas ID | HS095-32110 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chrX:13438460-13439630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chrX:13439156-13439167 | AAATCACAGCC | + | 6.02 | | MEF2C | MA0497.1 | chrX:13438820-13438835 | TGTTATTTTTAGAAC | - | 6.36 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAGCCTGGT AAAGACAAGA GGAGCTCAGA GAAGGGGCTC ACCCCCAGCC CGCAGTCCCT 60
ACTCACTTGC AGTCCCCATC CATCTCCCAA AGAGATGCTA TCTGCCAGTG AGCAGGGCGA 120
ATTGAAAATG GGATAATGAC AAGACTGTGG GAGGAGGCGA TTTCCAAGAT CAGTTCCACT 180
GAGACAGACT GTGAAACCCC TGGGGCTATT ATGACCTCTA ACTAAAAATG GTGGCAATGG 240
ATCTCTCTGG GCCTGTATGT TCTTGTGCAT AAGGCACCTT ACTCAACACA ATAGACAATG 300
ATCAGACAAG GACAGTGTGT GCATTTCAAG AAGCCTACTT CCAACACTGC CTCAACAATC 360
TGTTATTTTT AGAACATGAC TAGGAATTGT CTTCAACTGC CCAATTTCTG TTTCCTTCTA 420
ATCAGCCTCT TGAAAGACAG TACTGTATTC CTAAAGCAGA ATGTTAGAAG CACACAGAAT 480
ACTAGGAGGG ACAACACAGT CATTGTTAGG AGGGCTTAAA AGAAAGAAAG GGCTGGGGAT 540
AGTCTTTGGG CCTGTTTTGG CAGGTACCAC GGTTCAGGAG TCAGGTAGGT AAAAGTTTAC 600
CAGTTGGAGA ACTTTCTGTT GTGCTGAGGG CCATCACGCA AGGTCTGAAA ACGGAACAAG 660
CCTGGGAGTA GATGTGCTGT GTATACAGCA ATGTGGAAAT CACAGCCACA GGCGAAGCAT 720
TTGCCTGTAA TGACCATACT TGCTCAGTTT GCCATAACAT ACATAACATA TGTAAATTAG 780
CACTTAATAC ACACCCATTA GGGACAAAGA TCTGAAGTTG TGTGGACTCT AAATGGAAAA 840
GGTACTATGA TTGAAAAATA ATAGTCTAGG GCTTGGCACG GTGCCTCACG CCTGTAATCC 900
CAGCACTTTG GGAGACCCAG GCGGGTGGAT CACCTGAGGT CAGGAGTTTG AGACCAGCCT 960
GGCCAACATA GCGAAACCCC GCCTCTACTA AAAAATATAA AAAATTAGCT GGGCATGGTG 1020
GTGGGCGCCT GTAATCCCAG CTACTCGGGA GGCTGAGGCA TGAGAGTTGC TTGAACCCAG 1080
GAGGCGGAGG TTGCAGTGAG CCAAGATTGT GCCACTGCAC TGCAGCCTGG GTGGCCTGGG 1140
TGACAGAGAC TCCATCTCAA AAAAAAGAAA 1170
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