| Tag | Content |
|---|
EnhancerAtlas ID | HS108-09317 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr12:42758070-42759740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr12:42759270-42759280 | AACATATGTC | + | 6.02 | | RUNX1 | MA0002.2 | chr12:42758958-42758969 | GTCTGTGGTTT | + | 6.62 | | ZNF263 | MA0528.1 | chr12:42759475-42759496 | TCTTCCCTTCCTCCATTCTCC | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAAGTATTA TATAATGTTG AAAAATATGG AACAAGAGTG TCATCAAGTG GCCAATATAC 60
TTTACTTTTA AATGCTAGGG GCTGGGTGTG GTGGCTCACA CCTGTAATCC CAGTACTTTG 120
GGAGGCTGAA GTGGGAGGAT AGCTTCAGCC CAGAAGTTCG AGACCAGCCT GGGCAACATA 180
AGGCGACCCC ATTTCTACAA AAAAAATTAA AAAATAAGTT GGATGTGGTG GCATGCGCTT 240
GGTACCTTTG GAAGCTGATG TGGGAGAATT GCTTGAGCCT GGGAGGTTGA GGCTGCAGTG 300
AGCTGTGATC ACACCATTGC ACTCCACCCT GGGTGACAGA GTGAGACTCT GTCTCAAAAA 360
ATTTTTAAAA AGGCCAGGCA GGTGGCTCAT GCTTGTAATC TAAGCACTTT GGGAGCCCGA 420
GGTGGGTGGA TCACCTGAGG TCAGGAGTTT GAGACCAGCT TGGCCAACAT GGGGAAACCC 480
CATCTCTACT AAAAGTACAA AAATTATCTG GGTATGGTGG CATGCTCCTG TAATCCCAGC 540
TGCTCGGAAG GCTGAGGCAC GAGAATCACT TGGACCTGGG AGGCGGAGTT TGCAGGCGAA 600
GGCGTGCTGT TGCACCCCAG CGTGGGCGAC AGAGGGAGAC TCCGCCTTAA AAAAACAAAC 660
AAAGTTCTAG TTGGAAGATC TCTTAGTCCA TATCTTATGC CTGGAATACT TTCGTTTGTT 720
CTACTTTTTC TAGAATGCTT TTAACTGTAA ACATGTGATT TTGTGGAAAC AGCCTTGAAC 780
TTGACCACCA AACTTCTAAT CTGAACTCAA GCAGGCAGAC AGGTGTTTGA TTTTTTGATA 840
GGATAGAAGA AGAGGTGATA TGGAAAATTC CTCAGCTTAA GTCGCAGTGT CTGTGGTTTT 900
CCGTTTCCAC ATTTAAAATA AAAGATATTT GAGGTTGTAC TTCACTTATT CTTAAGCTTG 960
CCTTGCTAAT TACCTGGCTG CTTTCTCAAA ATAATTCTTG AAATCGTAAT TCTTTTTGGA 1020
AGTCCCTATT GACTAGAAAG GAAGTAGCCA ATATTTTATA TGAATATTTG TGTATATTTG 1080
GATGTGGGAA GGAGAGAAAA ATGAGGTTCA GAATAAGAAG TAAATGCTTT CCATCTCCCC 1140
ATTCTTCCCT TCCCTTGTAT CCCTTTCTCC CACTTTGTCG AATTTTACTC ATAACCGGTG 1200
AACATATGTC TGCTGACACT GAGGGTTCTA TCACCGCTTA CCTGGTTTGA CTGATGTGAG 1260
GGGCGGGAAT TACCTTGGGG ATTTGTATTA ACAGGAGAAT CTGAGCTTCA AAAATCTGCT 1320
TTTCAAATAA GCATCTAAAG TAATCTGCAA TCACAGATGG TTCAAGGACC ACATTTTGAG 1380
AGACAGTGCC TTATGGGGTG TTAGTTCTTC CCTTCCTCCA TTCTCCTGAT GACTTTGCGT 1440
CTTTTATATG CCAGCCAGTA TAGCTGGAGT GTTTGCGATA TAGCCAAAGA CACTGTCCTA 1500
ACTCTCAGGC TGTGTACTCT TTGATAATAA AAAGCATCAG TTTCGTCAGA TGTGTTTTTT 1560
GGAGGCCTCA TAATCCTGGT TGTATTGTTA TTTATATTTC TTCAAAGGCC CTTTTTGATT 1620
CATCGTATAG TTCATTGTAT TGAATGCATT GTATCATATA TGTTGATACC 1670
|
| |
|
|
|
