Tag | Content |
---|
EnhancerAtlas ID | HS134-03272 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:155101230-155102820 |
Target genes | Number: 24 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:155102149-155102160 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:155102149-155102160 | GGGTGACTCAG | + | 6.02 | ZNF263 | MA0528.1 | chr1:155101397-155101418 | GGAGGAGCAGGGAGAGAAGTG | + | 6.54 | ZNF263 | MA0528.1 | chr1:155101759-155101780 | GGAGGAGGAGGGGACAGGAAG | + | 7.15 |
|
| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_06471 | chr1:155096466-155104728 | Brain_Hippocampus_Middle | SE_07527 | chr1:155096600-155104005 | Brain_Hippocampus_Middle_150 | SE_23168 | chr1:155096831-155104699 | Colon_Crypt_1 | SE_23913 | chr1:155096865-155102477 | Colon_Crypt_2 | SE_23913 | chr1:155102493-155103155 | Colon_Crypt_2 | SE_25038 | chr1:155096824-155103109 | Colon_Crypt_3 | SE_26314 | chr1:155097879-155104734 | Duodenum_Smooth_Muscle | SE_26817 | chr1:155096813-155103510 | Esophagus | SE_27749 | chr1:155096773-155104848 | Fetal_Intestine | SE_28639 | chr1:155096730-155104902 | Fetal_Intestine_Large | SE_31531 | chr1:155096816-155104839 | Gastric | SE_34608 | chr1:155099429-155103501 | HCT-116 | SE_35043 | chr1:155095845-155105030 | HeLa | SE_36485 | chr1:155099148-155103878 | HMEC | SE_40872 | chr1:155098208-155104773 | Left_Ventricle | SE_41746 | chr1:155096958-155103454 | LNCaP | SE_42320 | chr1:155096778-155104870 | Lung | SE_47900 | chr1:155098283-155103087 | Pancreas | SE_49199 | chr1:155097092-155104701 | Right_Atrium | SE_49607 | chr1:155100275-155103472 | Right_Ventricle | SE_50340 | chr1:155096805-155104715 | Sigmoid_Colon | SE_52513 | chr1:155096836-155104823 | Small_Intestine | SE_56988 | chr1:155096855-155103515 | VACO_400 | SE_57550 | chr1:155099144-155103474 | VACO_503 | SE_58142 | chr1:155097801-155103164 | VACO_9m | SE_65093 | chr1:155099051-155104035 | NHEK | SE_65444 | chr1:155096946-155105042 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 155102278 | 155102800 | chr1 | 155102800 | 155102816 |
|
Enhancer Sequence | GGTTACAGAA GGTTCTGGGC AGGAAGGAGT TAATTTCTCC TGGGCAGGTT TAGGGCTGTG 60 AGGCAAATGG TACTGGGAGG AAGACTCTGT CGGCCCCTTT GTTCTTGCCC TTGAGTTTTC 120 TGAAGTTATG GGAACAATAT TTGAGGGAAT ACAGGAGAGG GTGGTAGGGA GGAGCAGGGA 180 GAGAAGTGGG CAGCTTGGTA TCACGAAAGC CATCTCACCG GCTTAGCCAC TCTCGGCCCT 240 AGCAAGCTTG CCCCCCACTC CCCTTGAGAA ATATGTTGTG CCAGCTTCCT CTGACCCCGT 300 GTCATCGTCT GGTGAGGCAG TCTGTTGTCT GTGGCTTGTT AGGGTGGGGG AGAGAACAGC 360 CAGCTGCCAA CCCCAGAGGG CAATGCCCTC CTGCCCATGG ACGCTGGGGA GGCTCAGCCA 420 GCCCTCCGCC ACCCGCTCCC TGTGCTTTGC CTCCTTGACC TGATGCATCT CGCCCTAGTA 480 TGGGAGAGAG CAAAGTCCCT GTTTATGCCC ATGCCAGGTG TTGACTGGAG GAGGAGGAGG 540 GGACAGGAAG CCATGAGTAG GGAGGGGGGG ACCCTGGCCT TTTCCGTTCC CAAGCTCCCA 600 GGTTTCCTCT CTTTCAGGAA GGAGCCTCTT CCTTACCCAC CTCCCCGCCT TCCCTGACGC 660 CGCTGCCCCC CTTTCCCAGA TGGGGAGCAA GAGTCAAATG AAGGCTAAGT ACAGCAGACT 720 GTACCCCCAG GAGAGGGGGC TGATGGGTGA CCCTCTGGCC ACACACACAC ACACACACAC 780 ACACACACAC ACACGCACAC CCTATCATAC CCAGGACTAA AGAGACGCCA GTCCAGAGTA 840 GAGTCCGTAG GCAGCCAAGC TGGGCCCAGC GTGGGGGCAA ATATGAGGCT ACAATGAACG 900 GGGTAGGTGA GGCTGGCATG GGTGACTCAG GCCAGTGGGC AGCAGCCCTG GGATCTCCAG 960 GCCTCAGGCG GGGGCAGCAT GCTGAGAAGG GCGCCAGCCT CCCTCATGCT GGAGGGCAGG 1020 CCCCTCATTC TGACCTGCCA GCTCCCTTTG TTTGGAGGAC ACTGTTGGGG GTGAGTGGGC 1080 GCTGTGCCCT CCTGGGGTCC TGGGGGCTGT GCACATTTGA CAAGGTAAGT TTTCACAAGT 1140 TCTCATGAGT GCTGGGGCGG GTAGCAGAGG TGGATGAGGA ATGAGTCAGT GCCCGTCACG 1200 GGAATGAGGG AAAGACGCCA GGCCCAGAGC TGAAATACCT GTTCTGAAAT GGCTTCTATG 1260 TTTATCTCTC CAGAGAGGAA TTTTAAAAGC CTCTCTCTGC TCCTCTCTTT TCCCCAGGGT 1320 GGGGGAGGGG CCTGGTAAGC CCAGTTTGGG CGCTGGCACG CTGCTGCAAA GCCTGGCCTC 1380 TCAGGGGTCA TGCTGATTGG GCAGTGGGTG CCCACCTCCG AGTCCTCTCT GCCTGACTCC 1440 TTCCTCGCCC TCCCAGCCGT GGCCAGGGCT TTCAGTTCGA AGCAACTTAG CGCTAATTCT 1500 GCTGGGTCTC TAGCTGGCAG TGCCTGGGGG AATTAGAGAA ACTGACCAGC TTGCGGGGTC 1560 GGGGGAAGCA CTTTTCCCCC TACTGGGACC 1590
|