| Tag | Content |
|---|
EnhancerAtlas ID | HS176-16180 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:29697540-29699860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr17:29698649-29698660 | TGATTAGATTA | - | 6.32 | | IRF1 | MA0050.2 | chr17:29698506-29698527 | GCTTTCTTTCAGTTTTGTTAT | + | 6.19 | | Myog | MA0500.1 | chr17:29699388-29699399 | CTGCAGCTGTT | - | 6.02 | | RARA(var.2) | MA0730.1 | chr17:29698992-29699009 | AGGTCATCCCAAGTTCA | + | 6.81 | | Tcf12 | MA0521.1 | chr17:29699388-29699399 | CTGCAGCTGTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 29697887 | 29697956 | | chr17 | 29699380 | 29699430 |
|
Enhancer Sequence | TTTGAGGTTT GACGGTTATT TGCTTCACAA AACAGAAAGT GGAATGTTCT TAGCACTTTT 60
TTGAAGATAC CTTCACCCTA GTGACTTCAT CTACATTACT ACAATTTATG TAATTGTAAT 120
TCTCAGGAAT AACACTGTGC CCAAACAGAA GCATTGCCAC CCATGTCATG ACTGTTTTCC 180
CCTCAGAGTA GGCCATGGTC TAGTAGTAGC AAGACACACA AGAACGAGCC CCAGGGTAGC 240
AGATTGCTGG CAGAGAGTCA CAGGGCCTTC CTAGTGGTCA TCCATGCTTC ATGCCCCTCC 300
TGCATGCGGG CCAGCTCCAA GTTGTTTCAA ACCTTTGTCT TTTTAAGGTC CTAGTTTTGC 360
CTGAATCTTA TTTTCTATTA AAGAAACAAC TCAGAATTAC TGGACTTGAA ACTTGTAGGC 420
CAAATGCAAA TTTGAGGAAA TGGAAGGTCA AATACGCTGA CAAATTCATA ATTTTAAGTG 480
GAGGATGCCA AAGGGAAAAA AAAAAGTTCT ATCTTTTCAA CTAAAAATAT TATACCACTC 540
TCTGGAGATC AGGGATTGCA TGCTTTGGGG CTCTGAATTA CAGGTATCTA GCTATCACAT 600
TTTAAAATGG AAGTGTTCAG TTCATTCAGT ATTAATTGAA AATAATTTTT CAATGTATTG 660
AAAAAATAAC TAGATTTTAC AGGAAAACAA AAATGAATAA TAATGATCTT TACCCTTCTC 720
AGTGCCTTTA CTCAGTAGAG GAAGATGGAT GTACAAGTTG TAGAATCATA GGCAAGTTAA 780
TTTAAAAGCA AGGAAGGAGA AAGTAGTTCT GGCAAGAGAC AGAATAATGC ATCATGAAGG 840
AAAAGGATAT GAGAAAAAAA AATATGGGTT GAATTTTATC TTGTAGAGAT ACGCAAGACA 900
ATTAAAAGAG CCTACACAAA CATACATCCC AAAGAAGCTC AAGGCACATT CCAGAGATCA 960
TGAGCAGCTT TCTTTCAGTT TTGTTATTTC TTTTGTAAAT AGCTCTGGAG AGGATGCAAA 1020
TAAATATACA GAAGAGAATT TAAATAGACC AGAATTCTGT TACCCAGAGA AAAGTTCCAT 1080
GAATGTTTCT AGTCATCTTT CTATGCATAT GATTAGATTA GATTAGATTA GAACATGACT 1140
AGCCTTAAAA AATTTAATAA GGGTTTTAAA AAAGATTTGA ATAGAACAGA TTTTCAGTGG 1200
TGGTTCAGCT ATGCTCACCT CCTGGAGAAA TGTCGCTGAT GTTTTTCCTT GCACTCATAT 1260
GCCTGATGCA GTGCACATGT TCATAAACAG TCACTGACAA ATGCCCATGT TCCTTTGACA 1320
GCAGTTCAGA TTTTCAAGAC AGCAAATCTC TGTTGAGCAC GTGTAAACCA GGCCACGTGC 1380
TTACAGATGC CTGATACTCT TGAGTCGAAT TCAGAGCTGA ATCCAAATGA AAGATGAGTG 1440
GCTCCTAGAG GGAGGTCATC CCAAGTTCAT TTCCTGTTCA TGAGCCAACA AATAACTAAC 1500
TGGGTAGATC TATGTACATT TTCTGTAACA TAATGAATAC TTCTTGACTT GAAATATTAC 1560
TTTTTGTCCA AAAATGGAAA TTTTTCTATT CTAAGATTTA AAATTTCAAT ATATAAAGAA 1620
GAATAAAGTA CAAATTAGCT GAAATCTTGC CATACAGAGG TAAAATATAT TTTTTAGTCC 1680
TTTGGCTTCT GACAGAGATA AAATATTTTG GCAGATGTTT ACCCAGCCCT ACGCCCTCTC 1740
CCCACAGTGT GTGGGTGTTT TTTTCCTACT CCAAAAATTG TGGTCATCTT TTTGTATCAG 1800
TAAATATCAA TCAGTAATGT ACATTTTGAT ACAAATTACT AAAACGTTCT GCAGCTGTTT 1860
GCTTTCCCGC CAAAATTTAT GCCAGCAGTA AGTATAATCA GTCTAATTTT GGGGGTAAAT 1920
TTTATTGATG TTTAACAGAA AAGTTCACAA ATTGCAAGTT TTCAGCTTAG TGAACTTTTA 1980
AAATGTAAAC ACACTTGAAA ATCCATCATC TACATCAAGA AACAGAACAT TACCAGCATC 2040
CCAAGAAGCC ATCCTCATGC CCCCTTAAGT CACTACTTCC GCAAGGGTGA CCACAGTCCT 2100
GTTACCCAAT TTGTAATCTT TCCTAATGTG ATAGATAAAA ATAAAAATCT TATTTTAGTT 2160
TCTGGTTACT TTTCTGAAGT TACTGCTTAG ATTATTTATA ATATTAATTG GGGTGGGGTG 2220
CAGTGGCTCA TGCTTGTAAT CCCAGAACTT TGAGAGGCCA AGATGGAAGG ATTGCTTGAG 2280
ACCAGGAGTT CAAGACCAGC CTTGGCAACA TAGTGAGACT 2320
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