| Tag | Content |
|---|
EnhancerAtlas ID | HS052-16699 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:66048740-66050080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr17:66049190-66049200 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr17:66049190-66049200 | GACACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_38542 | chr17:66048585-66052351 | HUVEC | | SE_44541 | chr17:66048716-66051358 | NHDF-Ad |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 66048744 | 66048806 | | chr17 | 66049017 | 66049264 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I068052 | chr17 | 66048744 | 66051971 |
|
Enhancer Sequence | GATAAGAGAA TAAAAGCAGG CTGCCCGAGC CAGCATTGCC AACCTGCTGA GGTCCTCTTA 60
CGCGCCATGG AAGCTTTGTT CTTTTGCTTT TTGCCATAAA TCTTACTACT GCTTAGTTTT 120
TGTGTCTACG GTGTTTTTAA AAGCTGTAAC ACTCGCCGAG AAGGTCTGCA ACTTTCACTC 180
CTGAGCCCAG CGAGACCACA AGGCCGTCGG GAGGAATGAA CAACTCCAGA TGCGCTGCCG 240
TAAGAACTGT TAACACTCAC CGTGAAGGTC TGTAGCTTCA CTTCTGAGCC AGCGTAGACC 300
ATGAACCCAC CAGAAGGAAG AAACTCCCAA CACATCTGAA CATCAGACAG GACAGACTCC 360
AGACACGCCT CTTTAAGAGC TGTAACACTC ACAGCGAGGG TTTGCAGCTT CGTTCTTGAA 420
GTCAGTGAGA CCAGGAACCC ACCAGTTCTG GACACGTGCC CACCGTGGCC TCAAAGTGCT 480
GGGATTACAG GCATGAGCCA CTGCACCCTG TCGCTTTTTT TTAAATGTCA CTCCCTGATC 540
CTAAGTAGTG TAAGACCTCA GATGAACGAA TGTAACTGCC ATTGACTAAA GAACTCTAGT 600
TGGACAGGCG TTTTAGCTGT TGTCCTTAAA AGATGGCCTT TGGTTGACAT TCGTTCCAAA 660
AGCATGATGA AACACTGAAA ACTTGTGTGG TTCCTTTGTC CCAGGAAAGG GAAGATGGCA 720
AGGGCTTATA TCTCGTTTGG CAAGGAGTTC ACAGTTTCCC TGCAAGCCCC AGAAGGTGGG 780
TGGTAACAAT GGGATGTGTT TGGCTCCTCA TCCTCCTGCT GACAGCCAGG TCTCAGAGAG 840
GCAAGTCCCA CACTTCCCAA GCTCTGGATC CGAGCTTCGC TGCCGCAGAA GGAAAGTCTA 900
ACTAGTTAGG AAGCACAGAA CTTGCCTGGC CTTCACCAGC ATAATCAGAT CTGTCATTCT 960
CTTCAGGAAC TGGCTCTGCT CTAGGCCTTG TTCTTTGCTC TGGAGGTAAC AATTGCCATT 1020
TTTCTTTGGT ATTTCTGCTG TAGTGATCAT ACTTGCCCTT CTCATAGGAA ATCATGGGAA 1080
TCAGCCCCAG TCACAGCTGG CTCCCAGATG GCTCTTGATC CTGTGACCCC ACCAACATTC 1140
CAATGCGATT TGCTTGGGAG GTTCAAACTT GGCTTGCTGG GGCACCATTC TTCTGGAACC 1200
CCACCCTGGG AGATTTATAG GCAGGCCTTG GAGAGAACAA ATCTCTAGAG GTGGGATGGG 1260
GCCAAGCAGT TTCCTTGTGT TGCATGTTCT AGAATTCTGC CTAAAACAAA AGAGGCTGAC 1320
CTCATTCTTG CCCCACCCGA 1340
|
