| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11187 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:80839260-80842020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:80839796-80839814 | CCTCCCTTCCTCCCTCCC | - | 6.88 | | EWSR1-FLI1 | MA0149.1 | chr17:80839792-80839810 | CCCTCCTCCCTTCCTCCC | - | 7.28 | | EWSR1-FLI1 | MA0149.1 | chr17:80839800-80839818 | CCTTCCTCCCTCCCTCCC | - | 7.28 | | KLF5 | MA0599.1 | chr17:80841023-80841033 | GCCCCGCCCC | + | 6.02 | | TFAP2C | MA0524.2 | chr17:80841573-80841585 | TGCCCCGGGGCA | + | 6.74 | | TFAP2C | MA0524.2 | chr17:80841573-80841585 | TGCCCCGGGGCA | - | 6.74 | | ZNF263 | MA0528.1 | chr17:80839787-80839808 | CTCTCCCCTCCTCCCTTCCTC | - | 6.13 | | ZNF263 | MA0528.1 | chr17:80839783-80839804 | CCCCCTCTCCCCTCCTCCCTT | - | 6.75 | | ZNF263 | MA0528.1 | chr17:80839799-80839820 | CCCTTCCTCCCTCCCTCCCTC | - | 7.19 | | ZNF263 | MA0528.1 | chr17:80839788-80839809 | TCTCCCCTCCTCCCTTCCTCC | - | 7.21 | | ZNF263 | MA0528.1 | chr17:80839791-80839812 | CCCCTCCTCCCTTCCTCCCTC | - | 7.22 | | ZNF263 | MA0528.1 | chr17:80839795-80839816 | TCCTCCCTTCCTCCCTCCCTC | - | 7.6 | | ZNF263 | MA0528.1 | chr17:80839780-80839801 | CTCCCCCCTCTCCCCTCCTCC | - | 8.13 |
|
| | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
| SE_02968 | chr17:80839220-80840814 | Bladder | | SE_25397 | chr17:80835597-80848538 | DND41 | | SE_26549 | chr17:80838932-80841687 | Esophagus | | SE_31064 | chr17:80838757-80844702 | Fetal_Thymus | | SE_31475 | chr17:80838551-80843395 | Gastric | | SE_41612 | chr17:80838472-80839616 | LNCaP | | SE_41612 | chr17:80839730-80841991 | LNCaP | | SE_42693 | chr17:80837699-80843439 | Lung | | SE_47793 | chr17:80839931-80842326 | Pancreas | | SE_55429 | chr17:80839881-80843487 | Thymus | | SE_65913 | chr17:80838471-80843221 | Pancreatic_islets | | SE_69083 | chr17:80838489-80840925 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 80840475 | 80841074 | | chr17 | 80839771 | 80840190 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I082880 | chr17 | 80838791 | 80852684 |
|
Enhancer Sequence | GGTGCAGAGC TTCTGCAGCA TCCTGGGGAG GTCCCGGAAC GTGGGTCTGG GCTGTGCTGA 60
TGCTGGAGCA GCCAGCGGGG AGAGCTGCCA GGCCACTCCT GACAGCCCCG CACCCGCTCT 120
GGATGGAAGC TTCTCGCTCC CAGCCGATAC GGGCCTGCTG CCTGCTGCTG GGGCTGGAGG 180
GGCCCCTCTG CTTGAGCCTT GGGGTACCCC GTGCCTACGT GCCCTCCTGG CTTTGCCCAT 240
GGTTGGTGGC CGTGTTTTGG GCTGCGTTGA TGTCGTTGTG GAGCCCGCTC TGGGCCTCGG 300
CACGTCTGAG CTTGATTGGG GTGGAAAATG CACCTGGTGG TTTGTATTAT GTTGTTTCTG 360
TTTTATTTAA TTTCATTTGC CATTCTTATT TCAAAAGATG CTTCCTATGT TTATGCTATA 420
TTGTTAGTTT AACTTCCTAC CCTTTCCATC TATGAATTTC TGTTTTTATT GTGGTTCTCA 480
GTGACCACAC TCTAGGGGTC CTTTCTCTCT CTCTCTGTCT CTCCCCCCTC TCCCCTCCTC 540
CCTTCCTCCC TCCCTCCCTC CTAGGCAGAG CCTGTGAGAC TTGCAGGCAT TTCCCCAGAA 600
CCCAGGCCCT CTTGGCCATC TGGCTGCTGC CCCACCCAAC CTTTGGCCTC TCCTGGGGCT 660
CCTGGATGGT TGGGCGTCCC AAATCCCCAT CAGCAGAGCA CTTGGTCACA AGGCCCGAGT 720
CACATGCCCC AGCTTCTCCG AGGAAGTGCA GAGTCCAGCC GCAGGGAGGA CTTTCTCAAC 780
CGGCCCTGGG GCCAGCTGTC CTGCTCCTCC TTGTTTGCTG TGGGCTCACC TCTGTGGGCT 840
GCTCACTCAG ACCCACTCGC ACCCATGGGA CCTTCCCACC TGTTTCTCCT GCCTCCTTCA 900
GTCTGTGCCC AGCACCCCGC TGTCAAGCCC ATTCCCCCCC AGCCCCTGAC GTTGGACATG 960
CTGGAGGAGA CTGTGGCCCT GTGGCGTGTT CTGGGCCATC TCCAGGGCCT GGAGCGGGCA 1020
CCTGTGCCCA GCACTGGAGG CTGGGGGACA AGTGCTCTCT CTGATAAATG CCCCCGAGTT 1080
TCAGTTCTGT GGCTGTAGTT TGTAGGTCTC CTAGCTCAGC ATCCCCGAGC CCATGCCCTG 1140
GGGACTCATG GGGCCGAGGA GAGAGGAGCG CAGAGAACAT GAGGATACGT GAGCCCCTTG 1200
CCTGAGAGGT GTGCTGTGAA CCTGGAGAGC AAGGCCAGTG GGTCTGGGGT GACAGACAGT 1260
GCGAGATGCA GGAAAACAGG CTCGAGATGC TGTGAATCTG GAGAACAAGT GGGCCTGGGT 1320
CTGGGGCAAC AGACAGCGTG AGACACAGGA GAACAGGCGG GATGCTGTGA AACCGGAGAG 1380
CAAGGCCAGT GGGTCTGGGT CTGGGTCTGG GGCGACAGAC AGTGCGAGAC ACAGGAGAAC 1440
AGACGGGATG TCATGTGCAT TGTGGCTGGC AGGGCCGGCG CCTCACACAC ACGCCCCGGA 1500
AGTCAGGATG TGGTGCTGAC GGTGTCCGCG CTGCCAGGCT GGAGCGGGTG ACGGTGCCTG 1560
CGCTGCCAGG CTGGAGCGGG TGACGGTGCC CGCCCTACCG GGCTGGAGCG GAGCTTGCTC 1620
TCTCTGCAGT GGGACCTGCT CACTTTTCCT TAGCTGGATG TATCTTTCAC ATTTAGCTTA 1680
ACAGCAGAGC TGGTGAGAGG ACGCACACCT GGCGTCACCA TTGTCCCCCG TGCATGTCCC 1740
CGGCGTCCTT CATGTTGACG CGGGCCCCGC CCCACGGCTC AGGTCTGTCA ACTTCCCTGG 1800
AACAAGGCAG AGCACTTGGC CCCTGGAAGA CCTGGAAACC AGGAACCTCG GAGGCGCTGG 1860
CGGCCTTGGA GGCCGCTTAT CTCCGCGTGT CTGAAATTCT GTTTTCCACC TTTTCCCTTT 1920
AGGCTGGTAG GAGGCGCAAT CTCTCAAGCC TTCCTTAGAA AGGATGATTG TCCTCCACCC 1980
TGCCCCAAAC CCCCTGTGTT CTGTGCAACG CCTGATGAGA GCGTTCTGGG TTATTCACAG 2040
TAACTGAGCT GGGTGATCTC ACAAGAGGAC ATAATGAAGC CCAAGGAGCC TGGTGGGGGC 2100
CGGGAGAGGC CTTGCTCTGA GTGTGGCTCG CATGGGGGCA GCGCCTTGGC GTCTGTGTGT 2160
GGTGCGGTGG TTTTCCTGCC ACTCTGTGGA AGGGGCCTCT GCCAGACGCC TTGTCTTCAG 2220
GGCCTCAGGT CCCTCTGGGC ACGGTGGGTG TTCATGTGTT TCTGCAGGGT TAGGCTCTGT 2280
GCATGGCGTG GTCTGCAGGA CCTGGACAGC CCCTGCCCCG GGGCATTTGT GTCGGCCACC 2340
TTGGTTTGCC CCCCTGTCCA AACGCTGCCA GTTCTCGTCC TCCAGGGCAC TCCGTTTCTG 2400
TCTTTTCATT CACTGGACCT CCCCACCTCC TGCGCCGCCC CACCACAGCA GGCCAGGTGC 2460
GTTCTGCCCC CAGGCCCTGT CCTCGTGGCT CTTTGATCCT GTGCCCTCGG TGTGCACCGT 2520
CTCGTGGCTC TCGTTAGAAC CAGGGTCGGC CACCCCCAGC TCCCACATGG CGTCTGGTGT 2580
CTTGGGGGTC ACATGTGTCT GTCTGCAGTC CCTGGGTGCC TCAAGCTGTG TGTTGCCTGT 2640
GGGGCATGTC TGAACCTCAA GTGGGCCTGA GTCGTGAGAG AAAGGCTTTC TCATCGATAC 2700
TGTGTGGTCT GTACTGTTTT GCAGAATTTC TTTTTAATTA ATCCTTTCTC TTTTTCACAG 2760
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