| Tag | Content |
|---|
EnhancerAtlas ID | HS176-16270 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:34948590-34950960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr17:34949023-34949034 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr17:34949023-34949033 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr17:34949020-34949035 | TCAGCCCCGCCCCCT | + | 6.06 | | SP2 | MA0516.2 | chr17:34949019-34949036 | CTCAGCCCCGCCCCCTC | + | 7.79 | | SP4 | MA0685.1 | chr17:34949020-34949037 | TCAGCCCCGCCCCCTCA | + | 6.4 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28134 | chr17:34947347-34959688 | Fetal_Intestine | | SE_29316 | chr17:34947369-34959574 | Fetal_Intestine_Large | | SE_52909 | chr17:34947399-34951928 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGCCGGGCCG AGGGCGGGGA CGTCGCGGGC GGGTCGTTTC CCCGGAGTCG GGTTCACCTG 60
CCCGCCACGC CGGGGCCCTT TGCTCTAGTC GGGGCGGCCT CTCGGATCCC TTAAGGCAGG 120
CTTCTCCCTT CCCCTTAAGT CTCATCTTTG AAGGAGCCGT TTGCCCTGAC AGCCCCTGCT 180
CGAGTTACCG AATCTCCGAC CCCGGCATCT CCCCACCCGC CCCTCGGGTC TCCCCAGGGT 240
ATTGGCCCGA GGAAGGGGAA GCCGGAGGTC GGGGGTGGTG GTCTCGCCCC TGTGGCCTTC 300
TCGCCCCCGG CGGCCAAGTG CCTCTAATCT CCAGAAGTCA CCCACCACGC AGGGCAAGGT 360
GGCTGGCCAA CCAGATGGGC AGGAGCCAGG ACTGAGGTTG GGGTTGGGGT GGGAGCTTTA 420
CTGAAGAGCC TCAGCCCCGC CCCCTCACCT CGGGGGTAAC TCATGCCCAG TGGCATGAGG 480
AATGAATGGA ATATTCATTA GTGGGCCCTC CTCCACTCTC CTGGGGCGAA CAGAGTGGGT 540
GAAATCGGGC GGAAACCTTG AGAGGATAAA GCAACCTGGA ACTCCTTACT CTGCTCTTGA 600
CGTGGGGTTG GGAGCCCTCA GAGCTCAGAG AAAAATCAAG ATGGCCATTT TGGAGCAGGG 660
AGGAATTTCT GTGCTAGGCT CTCTCTGGAT GTGCCCTGTA AGCTCATTCT CAGTGTCGGG 720
CTAGTGCTTA GCTGCAGGGC TTTATCTCCA CCGTGCTCAA AGTCCTCAGG CAGGGAAAGG 780
GTAAGGAGGC CTTGGGTGGG GGCAGAGGGA GAAGGTATAC AGGAAGGAGG ACTGTCCCCT 840
CCCCTGCTGC TGACCAAAGG TATGCTTTAT AACCCAGATA ATCCCAAGGT CACCTGGCTC 900
CATCACTGCC CCACTCTTTC CTCCCTTTAT CCTATTCTGA GGAGCTCAGG ACCCAGCCCC 960
AGCCTTGGAG CCCAGAGGAT CAGGCCAGGG ATTAAACAAC TGGATTCTGT AATTCTGAAG 1020
CCACTCTTGC CTTCTCACCT ACTCCCCTAC CGCAAGCTAG CCAGGAAGGG GGGGCCTGAG 1080
CCCCAAGGGG ATCCCCAGGC TGATCACTCA GTCCCAGGGT GACTCCATGT CTGAGAGGAG 1140
AATGCCCCTG TTGTGAGGGG GTGACATGAT GTTGTAGATC ATTACTGAGG GGAGGTAGGG 1200
AGATCAGGTG GCACAGGTGG GGCAACAGGA AGGCAGTGAC AGGGAGAAAT ACATTCTGAG 1260
CTCATCCCTT CTGGTTTTCT TGTGGCAGGA ATTTTGAGTC TAGAGGAGGA AGCGGGAAGA 1320
TGTACACCAG GGGAGGGGAA AGCTGCAGTC TTCCTTGCCC ACAGTCTGCT TTGATTGATT 1380
CAGTCATTGA TGTTAAAGCA GAATTTGGGT TCTAGCTTCC TACAGAGAAA ACTCCTGTTT 1440
CCTGAAGTGA TCAAATGTGG GTAAAATCTG GTGAAGGGGG GTTTCTGATT CTCAGAGGAC 1500
TATACCTTTT GAACTCACAG AAAGTCAAAG CAGAAAAGAA TGTCCCAAGA CACCCGATCC 1560
TGTCCTTTAT TCCTGGCTCA GCTTGGGAGG AGGAAGGGGC TCCAGGCCAG GGCAGCTGGC 1620
CAAGCTGGCC TTCCTCTAGG GCACCGCACG CCCCTTCCCC CTCGCCCACG TCTACACAGT 1680
CACCATCACA AGGCTCAAGT GCCCAGTCAC TGGCTTCCAA AGAAGGCCAC AGAACGTATT 1740
TTCTTCTTGC CTCTGAATGT CAGCTTCCCC CTGGGCTGCC TCTCAGTGGC TCTGCCTTCT 1800
CAGGTCTTTC TTGGCATGCT GAGGGCCTGG AGATGCACAG GGGGTGTTCA ATGGCACCTG 1860
CCACCTGAAT TGCCTCATAG TCTCCTGAGA AACCTCAGAG GGGAGGGTGG TGCACCAGGG 1920
CTCAGAGAGA AAGAATCTGT CCTGACTTTC TGACCCCTCC TTTAGGTAGG GAGAGAAGAT 1980
TGGCAGCTGG GCTTGGTTGA AAGGCATGTC TGAGAACTCT GAGCCAGTTG GCTGCAGTTT 2040
GCGAGGGGAG GGGAATAGTT CAGAGATGAG GGACTGGCTG ACACAATGCA GAAGAAGCTG 2100
GGTTAACCAG CCCAGTGACT CTCGGGACTG GTGTAGAAGC ATGAAGTGGT GGAGAGGCGC 2160
ATATTACCTA TGGGCAGAAG AGGTGTTCCT GTTGAGGAAG AGGCAGAAAA GAGAGAGCAC 2220
TCCATTCTCT AGGTCCCTGG CCCCTGTTCC ACCCAGGACT TGAGTTTATT TATTTATTTA 2280
TTTATTTATT TGAGACACAG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG TGGCGTGATC 2340
TCAGCTCCTG CAACCTCCGC CTCCTGGGTT 2370
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