Tag | Content |
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EnhancerAtlas ID | HS180-04216 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:204416800-204418310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr1:204417337-204417347 | TTCAAGTGGT | - | 6.02 | Six3 | MA0631.1 | chr1:204417428-204417445 | GACAGGGTATCACCATG | + | 6.11 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00064 | chr1:204415801-204417319 | Adipose_Nuclei | SE_00064 | chr1:204417530-204422553 | Adipose_Nuclei | SE_03975 | chr1:204415223-204416998 | Brain_Anterior_Caudate | SE_04850 | chr1:204414465-204417204 | Brain_Cingulate_Gyrus | SE_04850 | chr1:204417565-204418666 | Brain_Cingulate_Gyrus | SE_05834 | chr1:204414554-204422838 | Brain_Hippocampus_Middle | SE_06778 | chr1:204414634-204417237 | Brain_Hippocampus_Middle_150 | SE_07775 | chr1:204414572-204417332 | Brain_Inferior_Temporal_Lobe | SE_07775 | chr1:204417757-204421412 | Brain_Inferior_Temporal_Lobe | SE_10255 | chr1:204417782-204418559 | CD19_Primary | SE_10905 | chr1:204414650-204438582 | CD20 | SE_25125 | chr1:204416348-204417318 | Colon_Crypt_3 | SE_25125 | chr1:204417816-204422942 | Colon_Crypt_3 | SE_26688 | chr1:204416875-204421560 | Esophagus | SE_28866 | chr1:204417158-204423024 | Fetal_Intestine_Large | SE_30246 | chr1:204415638-204416972 | Fetal_Muscle | SE_31610 | chr1:204417780-204422694 | Gastric | SE_34711 | chr1:204415846-204421729 | HeLa | SE_40776 | chr1:204415081-204417377 | Left_Ventricle | SE_40776 | chr1:204417564-204421617 | Left_Ventricle | SE_42225 | chr1:204414898-204417247 | Lung | SE_42225 | chr1:204417746-204421550 | Lung | SE_48201 | chr1:204414946-204421702 | Psoas_Muscle | SE_48746 | chr1:204414986-204417248 | Right_Atrium | SE_48746 | chr1:204417807-204421419 | Right_Atrium | SE_50149 | chr1:204415315-204422829 | Sigmoid_Colon | SE_51536 | chr1:204415200-204417241 | Skeletal_Muscle | SE_51536 | chr1:204417745-204423045 | Skeletal_Muscle | SE_52421 | chr1:204416678-204422949 | Small_Intestine | SE_58430 | chr1:204415099-204506026 | Ly1 | SE_59794 | chr1:204415680-204491493 | Ly4 | SE_62377 | chr1:204415291-204492168 | Tonsil | SE_65868 | chr1:204415035-204417231 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I204445 | chr1 | 204415101 | 204423341 |
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Enhancer Sequence | CTCCCTCACT TTCCCTCAGG TTCTTTGTAA AATAGCCCTG TTAGACTTGG TGATCTCTAA 60 AGTCCTTTCC AGCTATAACT CTCAGCAAAA AATGAGAGGG AAACAAAAAG AGAAAAAGAA 120 TGGACATGTG AGGAAGAGGT TCGGTGGAGA TGCACCTTGG TGAGGGGTGA GGGGACAAGC 180 CCCAGCCAGA ACTCTGAACA GAGGTGTCAC CCAGCTGAAA CACGGGGTGC ATCCAGGCTG 240 AGTCCGGGGT GACTTCCATG GGGTGCCAGA GGACACTGCT GCCAGAGGGG AGGCAAGACC 300 ACACACTGGG AGAAGGCCCT GGGACACTCG GTCCCTACTC TATGCCACCA GATGTTCATC 360 CTACTAAAGT ATCAGAGCTG AGTGAGCCAA GTCTCCAAAG GAGGTCTACT TTCTTTCATT 420 CAAAAAACTT ATTTATTTAT TCATTTATTT ATTTATTTTG AGACAGAGTC TTGCTCTGTC 480 ACCCAGGCTG GAGTGCAGGG GTGTGATCTC GGCTCAGTGC AACCTCTGCC TCCCCGGTTC 540 AAGTGGTTCT CATGCCTCAG CTTCCTGAGT ACCTGGGATT TACAGGCACC CGCCACCACA 600 CCCAGCTAAT TTTTGTATTT CTAGTAGAGA CAGGGTATCA CCATGTTGGC CACTCCTGAC 660 CTCAAGTGAT CCCCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTGCAGGCA TGAGCCACCA 720 CACCCAGCCT CATTCAACAA ATATCTATTG AATCCTAACA TGTGCCAGGC ATTTTCTAGA 780 GTCTGGGCAT AAAGCAGCAA ATAAGACAGA CAAAAATTAG CCGGGCGTGG TGGTGTGCGC 840 CTGTAGTCTC ATCTACTCGG GAGGCTGAAG TGGGAGGATG ATTTGTGCCT GGGAGGCAGA 900 GGTTGCAGTG AGCCAAGATT GTGCCATTGC ATTCCAGCCT GGGTGACAGA GATCCTGTCT 960 CAAAAAAAAA AAAAAAAAAA CCTGCCTCAG GGAGCTTTCA TTCTATGTCA ACATTCATAC 1020 TCCATACCAA AGTATCTCAT AACCACAAGA AGGGGAAGCT GGGAACTGAG AAGTGCACCT 1080 TGGGCGTGAC CAGCTCCTCC TCTTCTCCCT GGAGAATAGG TCCATCCTGC CAAAGCACTG 1140 AGTCACTGGC AGGGGCAAAG GTGTCCCCTC AGGCCCCAAG AGGACCCAGG TCAGGTTTGA 1200 TCAGACTTAG ACGTATGAAG ATTCAATACA AGGGACTCAG AAGCTGAGCC CTGAATGCAG 1260 AGGGTCTCAG ACCCCATCTT CAGGCTCCAC GAAATCAATT TAACCTCCAG GAGATGGGAG 1320 ATGGATACCC CAGAGCTCAC CTCACAATCC ACATCTAACC ATATTCCCTC AGTTGCTTCA 1380 GTCACATCAT CCTCCCATGC TTGAAGTTCT AGCACTCTCT CCTGCTGTCC CAGCCCAAAT 1440 CTCCAGGAGA AAAATGTAGA GTTGACTGGA ATGGTCTTGC TGGTGACTGG GAGGGAAGGG 1500 CTAAAGCCTC 1510
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