| Tag | Content |
|---|
EnhancerAtlas ID | HS122-01192 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:204416940-204418310 |
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 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_00064 | chr1:204415801-204417319 | Adipose_Nuclei | | SE_00064 | chr1:204417530-204422553 | Adipose_Nuclei | | 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_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 |
|
| | 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 |
| GH01I204445 | chr1 | 204415101 | 204423341 |
|
Enhancer Sequence | TCGGTGGAGA TGCACCTTGG TGAGGGGTGA GGGGACAAGC CCCAGCCAGA ACTCTGAACA 60
GAGGTGTCAC CCAGCTGAAA CACGGGGTGC ATCCAGGCTG AGTCCGGGGT GACTTCCATG 120
GGGTGCCAGA GGACACTGCT GCCAGAGGGG AGGCAAGACC ACACACTGGG AGAAGGCCCT 180
GGGACACTCG GTCCCTACTC TATGCCACCA GATGTTCATC CTACTAAAGT ATCAGAGCTG 240
AGTGAGCCAA GTCTCCAAAG GAGGTCTACT TTCTTTCATT CAAAAAACTT ATTTATTTAT 300
TCATTTATTT ATTTATTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAGGG 360
GTGTGATCTC GGCTCAGTGC AACCTCTGCC TCCCCGGTTC AAGTGGTTCT CATGCCTCAG 420
CTTCCTGAGT ACCTGGGATT TACAGGCACC CGCCACCACA CCCAGCTAAT TTTTGTATTT 480
CTAGTAGAGA CAGGGTATCA CCATGTTGGC CACTCCTGAC CTCAAGTGAT CCCCCTGCCT 540
CAGCCTCCCA AAGTGCTGGG ATTGCAGGCA TGAGCCACCA CACCCAGCCT CATTCAACAA 600
ATATCTATTG AATCCTAACA TGTGCCAGGC ATTTTCTAGA GTCTGGGCAT AAAGCAGCAA 660
ATAAGACAGA CAAAAATTAG CCGGGCGTGG TGGTGTGCGC CTGTAGTCTC ATCTACTCGG 720
GAGGCTGAAG TGGGAGGATG ATTTGTGCCT GGGAGGCAGA GGTTGCAGTG AGCCAAGATT 780
GTGCCATTGC ATTCCAGCCT GGGTGACAGA GATCCTGTCT CAAAAAAAAA AAAAAAAAAA 840
CCTGCCTCAG GGAGCTTTCA TTCTATGTCA ACATTCATAC TCCATACCAA AGTATCTCAT 900
AACCACAAGA AGGGGAAGCT GGGAACTGAG AAGTGCACCT TGGGCGTGAC CAGCTCCTCC 960
TCTTCTCCCT GGAGAATAGG TCCATCCTGC CAAAGCACTG AGTCACTGGC AGGGGCAAAG 1020
GTGTCCCCTC AGGCCCCAAG AGGACCCAGG TCAGGTTTGA TCAGACTTAG ACGTATGAAG 1080
ATTCAATACA AGGGACTCAG AAGCTGAGCC CTGAATGCAG AGGGTCTCAG ACCCCATCTT 1140
CAGGCTCCAC GAAATCAATT TAACCTCCAG GAGATGGGAG ATGGATACCC CAGAGCTCAC 1200
CTCACAATCC ACATCTAACC ATATTCCCTC AGTTGCTTCA GTCACATCAT CCTCCCATGC 1260
TTGAAGTTCT AGCACTCTCT CCTGCTGTCC CAGCCCAAAT CTCCAGGAGA AAAATGTAGA 1320
GTTGACTGGA ATGGTCTTGC TGGTGACTGG GAGGGAAGGG CTAAAGCCTC 1370
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