| Tag | Content |
|---|
EnhancerAtlas ID | HS088-03776 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:155100550-155102820 |
Target genes | | Number: 42 | 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 | chr1:155100671-155100692 | TTTTCCTCCCCTCACTTCTCC | - | 6.36 | | 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: 3 | Chromosome | Start | End |
| chr1 | 155102278 | 155102800 | | chr1 | 155101105 | 155102178 | | chr1 | 155102800 | 155102816 |
|
Enhancer Sequence | CCTCGAGACT CCCGCTGGCA GCCTGGGCTC CCGGCTGGCA CTACCCCACC GGGATAACTG 60
TCCCGGCCAA ACCCTGAGCT GAGCCTAGAG TAGATGACCG AGGTAGGAGG GCGGCTGTAG 120
ATTTTCCTCC CCTCACTTCT CCGTCATATC TGGGAGCACC CCACCCCGGG GCATGCTTGT 180
GTCTACTTGC ATGGGCTTAT ATCTGCCCTT CCCTTCCTTC TCTCTGGCAC CCCTATTACT 240
CTAAAGTGAG GGACTCATGC TGGGCAGTTC CTGCCTTCAG CATAGACTTC GCCCCTGGCA 300
GCCAGGGCCC TTGTTCCAGG CCCCCCACCC CCCCACTGTG AAAGCCTCCA CGCCTCTCCT 360
TGTGTGTCCT TTGGGTATCT GACCACACTG ACAGATACCT GGTGTGACAT CAAGAGTGCA 420
CAGAATGCTC AAGGTAACCC TGGAAGGACC TCTCAGGAGA GAGCTGGGCT GTAGGCATTC 480
ATTATGCATT CACCCTGTAT TTAAAGCAAA CCTGGAAAGT CCCTCACTAG GGGTCTTTTG 540
GGGTGGCATG AGTGAGGCAC ATGCTGTGCA TGGGTAGGCT GAGGGAATCA CCTGTTTATG 600
GGGCTCTCAA GTAGTAAAAG CGAAGAGCTG GGAGAGGGAG ATCATGGGAA AGCTTCAGAA 660
TGAACAGAAG AGGTTAAAGG GGTTACAGAA GGTTCTGGGC AGGAAGGAGT TAATTTCTCC 720
TGGGCAGGTT TAGGGCTGTG AGGCAAATGG TACTGGGAGG AAGACTCTGT CGGCCCCTTT 780
GTTCTTGCCC TTGAGTTTTC TGAAGTTATG GGAACAATAT TTGAGGGAAT ACAGGAGAGG 840
GTGGTAGGGA GGAGCAGGGA GAGAAGTGGG CAGCTTGGTA TCACGAAAGC CATCTCACCG 900
GCTTAGCCAC TCTCGGCCCT AGCAAGCTTG CCCCCCACTC CCCTTGAGAA ATATGTTGTG 960
CCAGCTTCCT CTGACCCCGT GTCATCGTCT GGTGAGGCAG TCTGTTGTCT GTGGCTTGTT 1020
AGGGTGGGGG AGAGAACAGC CAGCTGCCAA CCCCAGAGGG CAATGCCCTC CTGCCCATGG 1080
ACGCTGGGGA GGCTCAGCCA GCCCTCCGCC ACCCGCTCCC TGTGCTTTGC CTCCTTGACC 1140
TGATGCATCT CGCCCTAGTA TGGGAGAGAG CAAAGTCCCT GTTTATGCCC ATGCCAGGTG 1200
TTGACTGGAG GAGGAGGAGG GGACAGGAAG CCATGAGTAG GGAGGGGGGG ACCCTGGCCT 1260
TTTCCGTTCC CAAGCTCCCA GGTTTCCTCT CTTTCAGGAA GGAGCCTCTT CCTTACCCAC 1320
CTCCCCGCCT TCCCTGACGC CGCTGCCCCC CTTTCCCAGA TGGGGAGCAA GAGTCAAATG 1380
AAGGCTAAGT ACAGCAGACT GTACCCCCAG GAGAGGGGGC TGATGGGTGA CCCTCTGGCC 1440
ACACACACAC ACACACACAC ACACACACAC ACACGCACAC CCTATCATAC CCAGGACTAA 1500
AGAGACGCCA GTCCAGAGTA GAGTCCGTAG GCAGCCAAGC TGGGCCCAGC GTGGGGGCAA 1560
ATATGAGGCT ACAATGAACG GGGTAGGTGA GGCTGGCATG GGTGACTCAG GCCAGTGGGC 1620
AGCAGCCCTG GGATCTCCAG GCCTCAGGCG GGGGCAGCAT GCTGAGAAGG GCGCCAGCCT 1680
CCCTCATGCT GGAGGGCAGG CCCCTCATTC TGACCTGCCA GCTCCCTTTG TTTGGAGGAC 1740
ACTGTTGGGG GTGAGTGGGC GCTGTGCCCT CCTGGGGTCC TGGGGGCTGT GCACATTTGA 1800
CAAGGTAAGT TTTCACAAGT TCTCATGAGT GCTGGGGCGG GTAGCAGAGG TGGATGAGGA 1860
ATGAGTCAGT GCCCGTCACG GGAATGAGGG AAAGACGCCA GGCCCAGAGC TGAAATACCT 1920
GTTCTGAAAT GGCTTCTATG TTTATCTCTC CAGAGAGGAA TTTTAAAAGC CTCTCTCTGC 1980
TCCTCTCTTT TCCCCAGGGT GGGGGAGGGG CCTGGTAAGC CCAGTTTGGG CGCTGGCACG 2040
CTGCTGCAAA GCCTGGCCTC TCAGGGGTCA TGCTGATTGG GCAGTGGGTG CCCACCTCCG 2100
AGTCCTCTCT GCCTGACTCC TTCCTCGCCC TCCCAGCCGT GGCCAGGGCT TTCAGTTCGA 2160
AGCAACTTAG CGCTAATTCT GCTGGGTCTC TAGCTGGCAG TGCCTGGGGG AATTAGAGAA 2220
ACTGACCAGC TTGCGGGGTC GGGGGAAGCA CTTTTCCCCC TACTGGGACC 2270
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