| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15801 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:2250680-2252160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:2251873-2251888 | GGGTCACACAGACCT | + | 6.33 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65320 | chr17:2250793-2252229 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I002345 | chr17 | 2248962 | 2252509 |
|
Enhancer Sequence | GTGAACCATC ACACCCGGCC TCATTTTTTT TTTTTTTTTT TAAACAAAAT CCAAAAACTA 60
CCACTGTTGG GGAGAGGTCT TTGATATATC CTTTTATCCT TTTTATCTTA AAACATCACA 120
TCAAGTTTAC ATTTTTCTCT ATCATATGGT TTTTGGATTT TTTTTCATTT TAATATAAAG 180
ACTTACTGTT GAATTAAAGT ATAGGCTGGT ATCTCCTGTC GCCCCCTCCC CTGGAGGGGA 240
AGGTGCTTTT GTTTTTTCTT TTTTTTTTTT TCCAGATGAG GTCTTGCTAT GTTGCCAAGA 300
TTGGTCTCAA ACTCGTGGGC TCCAGGTATG CTCCTGCCTT GGCATCCCAA GTAACTGGGA 360
TTACAGGTGC ATACCACCGC CCGAGGTCCA TAGTGTTTTA TTTACCCTAT TCCGATTGGG 420
CACTGAGTTT GCATTTTAAC CTTTGGCTGG TAGAGCAGGT TTCAGAGGCT CACAGAGAGG 480
CTTCTGGCCA GGCAGAGCAG GTTCTCAGGC CAATCATATC TCCCAGGACC TCAGCCTCCC 540
CACCCCCCAG GGATTGGGGC AGACACCAGC CTGCCTCCTC AGTCACCAGA TTCCCTGCCC 600
TGCTGTGTGC AAGTGGGTCA ACATGAGGGT TGCTTCAGAC TGAGGATGAG CTGTAATTCG 660
AGAAGGGTGG AATCTGTGGA GCCGGGAATA ACATCAGGCT TTATTAACCA GCTCCCTGTT 720
GCTAGGCAGC TTTCATTAGC CAGGAAGGTC TGCCCTGCAG TGAGCTCCTT CAGGGAATGG 780
CAAGGAGATG CTAATAAGCT GGGAGAGAAG CCGGTGCTAG GGAAGGCTTG CCTCTCCCCT 840
GGGATATTGC AGCCAGCGAT ATTTCAGCAC ATTCTGAGAT TTGGACTCCA GGCAGTCTTC 900
AGCCTGTCTC TTTTCAGTAA AAGGGATTCC TGGAGGCTGA GGTGGGAGGA TCCCTTGCAG 960
GAGTTCGAGA CCAGCCTGAG CAAAAAAGAC CCCATCGCCA CAAAAAGGAG GAGCGGGTTC 1020
CTCCTCCTTC CCACCCACAG GGAATGAATA GCTCATTCTC TTGCTATCTA ACTCGTGCCT 1080
TCCATCTAGA AATGATCTAA GAGGAAGGAG GGAGCTCTGA AGGAGCTGAC TCCCCTCACT 1140
CTATCTTGGG GCATTGCGGA GGGCATATGG GGATGTTCAT AGCTGGGACT TTGGGGTCAC 1200
ACAGACCTGG GTTCACATCC TGGCTGTGCC ACGAAGTGTG TAGCCGTGCT TACTCATCTC 1260
TGAGCCTACC CCAGAAGGCA GATGTAAGGA ACAGAAGAGC AATGCAGGCA ACACACACAG 1320
CATGGATCTG AGTATGCAGA AGGTGCTCAA TCGCATTCTA CTTTGGTTTT TATTTTGTTT 1380
TGTTTCGTTT TGTTTGAGAT GGAGTCTCAC TCTGTCTCCC CGCTGGAGTG CAGTGGTGTG 1440
ATCATAGCTC ACTCAGCCTC GACCTTCTGG GTTCAGGCGA 1480
|
