Tag | Content |
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EnhancerAtlas ID | HS113-16061 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr17:73085400-73086590 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:73085633-73085648 | GAGGTCAAGAGTTCA | + | 7.64 | RARA | MA0729.1 | chr17:73085633-73085651 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_23417 | chr17:73082484-73085667 | Colon_Crypt_1 | SE_23417 | chr17:73086270-73086637 | Colon_Crypt_1 | SE_23967 | chr17:73083263-73085621 | Colon_Crypt_2 | SE_23967 | chr17:73086293-73086563 | Colon_Crypt_2 | SE_24792 | chr17:73083145-73085644 | Colon_Crypt_3 | SE_28092 | chr17:73081834-73090441 | Fetal_Intestine | SE_29107 | chr17:73081529-73090434 | Fetal_Intestine_Large | SE_31669 | chr17:73082504-73085761 | Gastric | SE_31669 | chr17:73085808-73088484 | Gastric | SE_34420 | chr17:73081514-73093766 | HCT-116 | SE_34880 | chr17:73081698-73093720 | HeLa | SE_49028 | chr17:73083315-73085673 | Right_Atrium | SE_50549 | chr17:73082431-73086709 | Sigmoid_Colon | SE_52733 | chr17:73081873-73089953 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TGGGTCACAT TCATCTCCTC TTTTGTGCTC AGCCAGAGGC TGGGTGAGGG TTCATGAACA 60 GGTTCTTGCT TATAGTGTGG AAGGGGTAGC AGGGTGGGGG GTGACAATAA AGAAGGGGGT 120 GATCCACTCC AGTGTGGTGT GAGGACCACT ATTAAGGTGA GAAAACAGGC CAGGTGCGGT 180 GTCTCACACC TGTAATCCCA GCACTTTGGG AGGCTGAGGC AGGCGGATCA CTTGAGGTCA 240 AGAGTTCAAG ACCACCTGGC CGATATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT 300 TAGCCAGGCA TAGTGGCGTG TGCCTGTAAT CCCAGCTACT TCGGAGGCTG AGGCAGGAGA 360 ATTGCTTGAA CCCGGGAGGC AGAGATTGCA GTGAGCTGAG ATTGTACCAC TGCACTCTAG 420 CCTGGGAGAC AGAGCGAAAC TTCATCTCAG AAAAAAAAAA AAAAAAAAAA AGGCGAGAAA 480 ACAGGAAGGA GGTGCAGCCC AGCCTGGGGT GGGAGTCAGG TTAGCTCCCA GGATGCTGCT 540 AGGGCTGAAT CTTCTTTTAA GACTACTCAG GAGCGGTAGT AAGAAGGAGG GAAAGAGTAG 600 AACAAGGAGA TCGATCTGTA CCTGCCTGTG AACAATTAAC TGAAATTACT CACTACCTTT 660 GCACCCGCCT AAGGGGTGAA TTTTTTCTTT TTTTCTTTTT CTTTTTTGAG ACAGAGTCTC 720 ACCGTCACCC AGGCTGGAGT GCAGTGACGT GATCTCGGCT CAGTGCAAAC TCCGCCTCCT 780 GGGTTCAAGG GATTCTCCTG CCTCAGCCTA GTTTTTTATT TGTAGTAGAG ACAGGGTGTC 840 ACCATGTTGG CCAGGCTAGT CTTGAACTCC TGACCCCAGG TGAGCCGCCT GCCTCGGCCT 900 CCCAAAATGC TGGGATTACA GGTGTGAGCC ACCGTGTCTG GCAGGGCTGA ATTTTGAAAG 960 ACCAGTTGAC TGGAGAAACC GCTCGATGGG AGGGGAGGCT GGAGAGCCGA CTGGGCATCC 1020 ATACCGTGTA TGTGACCTGG GACTTACTGG GAGTGGGAGA GGAGACAGGG AAGGCCATGT 1080 CTGCAGTGGG GGTCCCAGAG AGGCGGGGGA AGGGGGTCCT CAGACCTTGG TGGCAGAGTT 1140 TCTTTTCTTT TCTTTTCTTT TTTTTTTTTT TTGAGACGGA AGTCTCACTC 1190
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