Tag | Content |
---|
EnhancerAtlas ID | HS101-02783 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:153916870-153918770 |
Target genes | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr1:153917218-153917231 | ATGACATCATTCA | - | 6.41 | JUND(var.2) | MA0492.1 | chr1:153917217-153917232 | CATGACATCATTCAT | - | 6.33 | KLF4 | MA0039.3 | chr1:153917550-153917561 | CCACACCCTCC | + | 6.32 | RFX2 | MA0600.2 | chr1:153916916-153916932 | GGATGCCATGGCAACC | + | 6.08 | RFX2 | MA0600.2 | chr1:153916916-153916932 | GGATGCCATGGCAACC | - | 6.12 | RFX5 | MA0510.2 | chr1:153916916-153916932 | GGATGCCATGGCAACC | + | 6.33 | RFX5 | MA0510.2 | chr1:153916916-153916932 | GGATGCCATGGCAACC | - | 6.55 | ZNF263 | MA0528.1 | chr1:153918437-153918458 | GGAGGAGGCTGAGGAAGGAGC | + | 6.23 | ZNF263 | MA0528.1 | chr1:153916949-153916970 | CCCTCCTCTTCCTAGTCCTTC | - | 6.49 | ZNF263 | MA0528.1 | chr1:153918434-153918455 | GGGGGAGGAGGCTGAGGAAGG | + | 6.89 |
|
| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_07112 | chr1:153916510-153920184 | Brain_Hippocampus_Middle_150 | SE_13301 | chr1:153916379-153919168 | CD34_Primary_RO01480 | SE_13979 | chr1:153916328-153920017 | CD34_Primary_RO01536 | SE_17279 | chr1:153916800-153919789 | CD4p_CD225int_CD127p_Tmem | SE_19751 | chr1:153916106-153919855 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20550 | chr1:153916049-153920190 | CD56 | SE_22844 | chr1:153916133-153920212 | CD8_primiary | SE_27263 | chr1:153916630-153920158 | Esophagus | SE_41224 | chr1:153916145-153919925 | Left_Ventricle | SE_42677 | chr1:153916172-153920139 | Lung | SE_49113 | chr1:153916189-153919933 | Right_Atrium | SE_50562 | chr1:153916550-153920149 | Sigmoid_Colon | SE_53266 | chr1:153916690-153920078 | Small_Intestine | SE_53527 | chr1:153916236-153920284 | Spleen | SE_59593 | chr1:153916527-153921857 | Ly3 | SE_60702 | chr1:153916094-153937455 | DHL6 | SE_62719 | chr1:153916077-153937522 | Tonsil | SE_65739 | chr1:153916330-153917168 | Pancreatic_islets | SE_65739 | chr1:153917349-153918800 | Pancreatic_islets | SE_68155 | chr1:153917025-153964411 | TC32 | SE_68156 | chr1:153917025-153964411 | TC32 | SE_68157 | chr1:153917025-153964411 | TC32 | SE_68158 | chr1:153917025-153964411 | TC32 | SE_68159 | chr1:153917025-153964411 | TC32 | SE_68160 | chr1:153917025-153964411 | TC32 | SE_68161 | chr1:153917025-153964411 | TC32 | SE_68162 | chr1:153917025-153964411 | TC32 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CATCTGGAAT GGTCAAGTGG GAGAGAGATG AAGCAAGGAA GGCTGGGGAT GCCATGGCAA 60 CCAGGGTACC CTCTTGCTCC CCTCCTCTTC CTAGTCCTTC CAAAGAAAGG CAGGATAAGG 120 GGTCGGCCAA TCCTGAACTC TTCCCCCTGT GACATCACTG CCCACCACAG CTTCTTAAAG 180 AGACCAGATC CCTCCCACTT AATGGTCCTG GCACTCCCCT CAAAGAACCT AAACTCCACC 240 ACACACAGCT AACCTGAGCT ATGACATTCA CATTGTCCAT GTGTCCCTTT TAAAGGCTCA 300 CCAGTTATAA CATCACAGAG ATCACAATCT TTTTTGTAAT AGCCTTCCAT GACATCATTC 360 ATGCTGGCCA TGACATCATA CCAACCTTAC AGTCTTTTCA AGGGTTTCTG ACCTTCCTAC 420 TCTAGTTATG ACACCATAAG AACCTTGTGA TCCTGCCAAT GTTCTTAAAG AGCCCACTCC 480 TAGGTTTTTA AGAGGACCCC ATGGGTTTCT GAGAAAGCCC ACAAAACCCA AGCTTTAAGA 540 GTCTTTTCAA CGAACCCAAG TGTCCTTTCT CCTAGCTTAA CTCCACCAAT CTGGCCCAAA 600 ATCCAGTGTT CTCACACCTC CAGGATCCTT AGGTAGCTCG TTAGATCCAA AGCAGTTGTG 660 AGAGACAAGT CCCGGCCATC CCACACCCTC CACCATGGAG CCCAGAGACA GAAACAGGCC 720 CACAACAGCC TAGTTCTCAC CTGCCTCCAT GGCCCAACCC CGGGGAGTAG GAGCCCCAAG 780 GGTCCTGAGG CGCCCCAGGG TGCAGAAGCT GGGAAAAAGC CTGGTGGGTA GCTCGCAGCA 840 GGGGCCCAGA AGCGTGGGGG GTGCTTCAGA GGGGAAGGGA GGTTACTTCC TGAAACAGTG 900 GAGGGGAAGC TGCAACTCAG AGGAAGTCAG CCTATGGGTG TGTGTGGTGG CGGTGGCGGT 960 GGTGGGGTTA CCATTGAAGG TGCCAGCACA GCATTACGCC AAGTTGGAAT CTCAGACTAT 1020 AGGATCCTGA GCAAGGCAGA GGAGGCTCAG AATGGTTCCA GGATGTGCAG TCCTGCTAAC 1080 CTCCTGCTGT TCCCCCAGAG AACAGGGAAT AAGGAATCTC ATAGAGCCAG GCTGGCTTTC 1140 TTCATCACCT GGCCTCTGGA CACACACACA CACACACACA CGCACACACA CACGCACACA 1200 CGTACACACA CCAACCCCAG CTAAATTTAG ACTCCACTTC TGGGAGGTAA AGCCAGGAGT 1260 CAGCGTCAGC CTCTTGATTT AATTCTGGGG CACAGACCTG TCCCTCATCC ACTGAGGGCG 1320 AATGGGAGCC CTATGCCCAA GGCAGCAGGC AGAGGCCATT AGGTGGGACC TTCTGAGGGG 1380 CAAGTGGGTG GCACCCATCC GCAGGACCTG CGCACCGGGG CCTCCCCTCA CCAAGCCAGG 1440 GAAGAGTCCT GCAGAAAGCA GCCCTTTCTC CCTAGGGAAG ACAACGGGCA CAGGGCCCAC 1500 TCCGGGTCCC CACGCCCGCG TGCCGGGTGA CGGGAAGTTC GGGTTGGGGC AGAGGGCGCG 1560 CCGAGGGGGA GGAGGCTGAG GAAGGAGCAG GAGGGCAGAG AAGCAGGCGC GCCGGCGGCC 1620 GAGGACGTGA CGGCAGCAGC GCCGGCCGCC GCGTGACCCA AGCGGGAGGG AGGGCGGCTC 1680 CGACTCCGGC ACCCACGGGA GCAGAAGGGG GTGCAGGAGG CCGGGCACGG CGAGCTAATT 1740 GCGGGAGGTG CCCTCCCCTC CACTTTCACT TCCCCAGGAG AGAGGAACCG GAACCAGATG 1800 TGCAGTGAGG GACAGCAGCT GGGGGCCATC CCCCACCCCG CCTGCCGCCC GCGCTCCCTC 1860 CTGCCCGTCC CCGCCTGCCG CCCAGCCCGG TCCAGCCCCT 1900
|