| Tag | Content |
|---|
EnhancerAtlas ID | HS053-15179 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr16:30921430-30922810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr16:30921760-30921770 | GACATATGTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACACCTGAGT CAGAGAGAGG AGGGGCTCTG CGGGTCCCCC TGTCCTGTGT CTCTGGGGCC 60
TGGCGCTCCT GCCCCTCACT CACCCAGTGA ACAGCTCATG CTCTCTCCTC GGCTTCTTCC 120
TCTCTGCAGC CTCTGGGTCT TTCAGGACAC CTGTCCTTCT GCCCCTCAGG TGTCTTTATA 180
CCTGGGGCTG AGCCCTGGGG TGGCCCAAGA GGGAGGGAGG GAGTCACATC CTGGGGAGAG 240
GGGCAGGAGC AGGCAGGGCC CTGGCAAAGA ATGAGAGACA GACCTGGCCA CCAGACAGGA 300
CAGGGAGCGG GTGGGAGGAC CCAGAAGGGG GACATATGTT CCGCACGGGG AGGCCTCGTG 360
TGCAGAAGCC CCAGAGGAAG GAAATGGGTA GGGAAGGGGA CACAGATGGG ACCCCCAGGC 420
CCCTCCAGCT CCCAAACTCG ACCCTAAACC CTGGTGGCTG GGAGGGAGGG GGCGAGGGCG 480
TGATGGGGAT TATCCAGGGA CAAAGGGGCC GCCCCGCTCC CTGCTGTTCT GCAGGTCCTG 540
GGATCCAGTT TCCCAGAGGA GGCCGCCCCC TGCTCCGCCC CACAGGGACC CAGGCGCTGG 600
GCCCGGGCTC CCAAGGAGTT TGGAAAAAGG ACAGGAGGGA TGGTGTGTGA GCAACATCAT 660
CGTCCACACC CAGGTTCACC CTTAGGCACA GGAACAGTCA CACGTCTACA CAGGCATTGG 720
CACGTGGGCA CACACAGGCA TGAGCACACA CTTTCATGCG CTCATTCATT CAGGACTTAT 780
GGGCCCTGAC TGTGCACCAG TCCCTGTTTT AAGTGCTGGG GACAGAGTAT GGAACAAGAC 840
AGACAAAAAT CCGTGCCCTC GTGGAGCTGA CACTTTAGTA GACATGGGTA CATATATGTG 900
GGATCATGCC AGGCCTACAC ACATCACACA CACAGTCCCA GACACACGCG TGCACACAGG 960
GGAACCCATA GTGCATCCCT GGGGGCCCAG CCAGAGGCAC CTACACAGAG CAGACGTGGG 1020
ACACACACCT CATGCCCATA GATGCACGCA GAGGTGGGGA CCAGGGGTCA TGGGATCTGG 1080
CCACGTCTTA GCCTCTGATA CACTAGGAGA TCTCCTCCCT CTGCCCAGGC ACAACACACT 1140
TGGACTTACA CACACACACC TAAGACACTG TCCCTCGGGG AAGCCTTGCA GCAGAGGGGC 1200
AGGGTCGGAG AGGCAGATGC TGGGTTCTGG TCTTTCTCCA GTACTCCCCC AAACTCTCCA 1260
TCATGGAACC AATGTTAAGT TCTCATCCCT GCCACCCCCT GAGTCAGGCA GTGATCGGTC 1320
AGACTCCCAC CCTAGTGGGC TGGAATACTG CTCCACCCTA GCTTCCCTGG TCAGGTGGTA 1380
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