Tag | Content |
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EnhancerAtlas ID | HS197-11489 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr2:47193520-47196530 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr2:47193953-47193969 | AATTCCTAGAAAGTAG | - | 7.14 | BCL6B | MA0731.1 | chr2:47193951-47193968 | TAAATTCCTAGAAAGTA | - | 7.23 | JUN(var.2) | MA0489.1 | chr2:47193617-47193631 | ATGAGTCATTTTTC | - | 6.68 | Myog | MA0500.1 | chr2:47195102-47195113 | CTGCAGCTGTC | - | 6.62 | Nr2f6(var.2) | MA0728.1 | chr2:47194135-47194150 | GAGGTCAGGAGTTCA | + | 6.22 | Tcf12 | MA0521.1 | chr2:47195102-47195113 | CTGCAGCTGTC | - | 6.14 | Zfx | MA0146.2 | chr2:47196402-47196416 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_00056 | chr2:47193106-47196568 | Adipose_Nuclei | SE_00864 | chr2:47194770-47195906 | Adrenal_Gland | SE_01547 | chr2:47194919-47195899 | Aorta | SE_03864 | chr2:47194593-47196000 | Brain_Anterior_Caudate | SE_04790 | chr2:47194452-47196092 | Brain_Cingulate_Gyrus | SE_05773 | chr2:47194415-47196333 | Brain_Hippocampus_Middle | SE_06717 | chr2:47194864-47196105 | Brain_Hippocampus_Middle_150 | SE_07731 | chr2:47194478-47195922 | Brain_Inferior_Temporal_Lobe | SE_09141 | chr2:47188826-47202968 | CD14 | SE_26122 | chr2:47194205-47196331 | Duodenum_Smooth_Muscle | SE_26616 | chr2:47194256-47196364 | Esophagus | SE_34911 | chr2:47193577-47196531 | HeLa | SE_36729 | chr2:47193948-47196530 | HMEC | SE_43054 | chr2:47194681-47196092 | Lung | SE_47823 | chr2:47194916-47195888 | Pancreas | SE_53025 | chr2:47194788-47196340 | Small_Intestine | SE_53323 | chr2:47194762-47195996 | Spleen | SE_54495 | chr2:47194376-47195982 | Stomach_Smooth_Muscle | SE_65159 | chr2:47193986-47196476 | NHEK | SE_65882 | chr2:47194784-47196030 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr2 | 47194314 | 47194923 | chr2 | 47196160 | 47196200 | chr2 | 47194379 | 47194775 | chr2 | 47195176 | 47195614 | chr2 | 47193730 | 47195806 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I046963 | chr2 | 47190740 | 47199767 |
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Enhancer Sequence | ATCTTTCCAG TCTTTTTTCC CTATAGGATT ATATATGCTT TTAAAATGTA AGTTCATACA 60 GTCATGTTTT ATAATCTGCT TTTTAAAAAA GTATTTCATG AGTCATTTTT CAATACACCT 120 CTATGTCACT GTAAGTAACT TCATAGCATT TCATTGTAAC GTTCTATCCT AATTTTGTGA 180 AGTCCCGTCA TTGGACCTGT ATGCTAAATC TTTTTTTTTT TTGCCATTAT AAATAATACT 240 GAAATGGATA TCCTTGAAGC TAAATTTTGT ATACATCACT TTTTTTTTTT TTTTGGTGGA 300 GATGGGGTCT ATGTTGCAAG GGCTGGTCCT GAACTCCTGG GCTCAAGCAA TCCTCCCACC 360 TTACCCTCCC AAAGTGCTGG GATTACAGGT GTGAGTCACC ACCCCCAGCT TTTTTTTTTT 420 TTTTTCGAAG ATAAATTCCT AGAAAGTAGA ATTACTGAAT CATAGAGTAT ACATTTTTTG 480 GAGACTTTGA TACAGAAGCC AAATTGCCTG TGTTTTTTGT TTTTTTTTTT TCCGTTAAAA 540 AATTGTGTTG GCCGGGCGCG GTGGCTCATG CCTATAATCC CAGTACTTTG GGAGGCTGAG 600 GCGGGTGGAT CACCTGAGGT CAGGAGTTCA AGACCAGCCT GGCCAACATG GCGAAACCCC 660 ATCTCTACTA AAAATATAAA AATTAGCCAG GCGTGGTGGC GCGTGCCTGT AATTCCAGCT 720 ACTCAGGAGG CTGAGACAGG AGAATTGCTT GAACCCAGGA GGTGGAGGTT GCCGTGAGCT 780 GAGATTGTGC CACTGCACTC CAGCCTGGGT GACAGAGCAA GATTCCGTCT CAAAAAAAAA 840 ATGTGTTAAA TATACATACC ATAGAATTGA CCATCTTAAC CACTTTTAAG CGTACAGTTC 900 GGTACTAAGA CACTGTTGTG CAACCAATCT CCTGAACTCT TTTAACATTT GCATTATTGT 960 GCAACCAGTC TCCAGAATTC TTTTACCTTG CGAAACCAAA ATTCTATGCC CGTGAAACAG 1020 CAACGCCCCA TTCCCTCCTC CCCTAACCCC TGGCAACCAC TCTTCTATTT TCTGTTTTTA 1080 TGAATTTGAT TACGCAAGTA CCTCATGTAA GAGGAATCAT ACAGTATTTG CCTTTTTGTG 1140 TCTGGCTCAT TTCACTTAGT AAAATGTCCT CAAGGCTTAT CCATATTGTA GCATGTGTCA 1200 GAATTTCCTT CCTTCTGAAG GCTGAATAAT ATTGTATTGT ATGTATGTAT ATGTGGCATT 1260 TTGTTTATGT GTTCATCTGT CAATGGACAC TTGGGTTGCT TCTACATTTT AACTATTGTG 1320 AATAATGCTG CTATAAATGC TAGTGTACTA ATACCTCTTT GAGACCCTGC TTTCTATTCT 1380 TTTGGGTATA TACCTGGAAG TGGAATTGCT GGATCATATG GTAATATCTA TTTTTAAATG 1440 TTCTAATTTT AACAGAGTGA TCTGTGAGGG TTCTTTCCTA CCTGGCCTTT CGGTTTCCCC 1500 CCGAGAGCTG AATGAATTGC ATTTTTTCGC TTCTTCCCGT GGCTGCAGGG TACCCAAGTC 1560 TGGGATTCAT CTTCCGTGGG TGCTGCAGCT GTCCTCGTGC CCTTTGACAG GCTGGGTAGG 1620 TGGGAGGGAA GGGGTTCTGT TGCTGAGGAT GTTTTCTGTT TTCTACCTCT GCATCCAGGG 1680 CCCAAGGCTC CAGGGTTCCA AGGGTGGGGC TTCTTGGAAG GGCGGCTGCC TTGGATGTGA 1740 TGAGTCATTC AGACTGAAGG AGTTGGGACC AGCCTGGTGT TGGGCCTGAG GCTGTGCCAG 1800 GATCAGCTTG GCTCCAAATC GAAAGTTCTG AGTTAATGAA AAAGCAAGTC CTCCTCTTGC 1860 AAGGGACCTT TCCTAGAGCT GGGTATTGGC ACAGAAAGGC CCTTGCCGGT GGGAATCACA 1920 AGGCAGTGCC TGCCCTGCAG GGCTGTGTTA CAACCCTCCG ATGCCTCAAG GACTGGGCGC 1980 AGGGCAGCCC ACCTTCATCC TGGATTGAGC ACTGTAGTCT GGCCGTTTGT GCAGAAGCGC 2040 TCACGGGGCA GAAGGTAAAG AAAAGAAACC CAAGCCTGCA GCACCTGGGT GGGCTTCCAG 2100 TCAGATGTTT GTGGACAGGA AAATAGACCT TATCAACCAG GGGACAAATA CAAGGTTCCC 2160 GGCCCCTTTT TATGGGCAGA ACTGGGTGAC TGGACTGTGA CCTTGCTTAG GAAAAGCCAC 2220 TGCCAGCTCC AGAAACTTTT TGGCCCTGTG TATATTGGAA ATTGCTTTAT AGAGGACCGC 2280 CTCCGTGAAT GTACCCCTCT ACTTTGAACT TTTATTTCTC TGAATCATGA CAGCTCCCTT 2340 CAAAAAGGCA TTATCTCCAT TATTTTTAGA TAAATTTTCA TATGGTGACA TGTACAAATC 2400 TTAACTGTAT AATTTCATGA ATTAGGCCAG TGTAAATATC CATGTGACCA GTACCCTAAT 2460 AAAGATACAG AACATTTCTA TCACCACAGA AAGTCCCCTT GGGCTCTTTT CTAATTGGTC 2520 TCCACCCCAG GCAACCTCTG TTTTGTTTTT GTGTTTTTTT TTTTTTTTTA AGAGATAAAG 2580 TCTCGCTATG TTGCCCAGGC TGGTCTCGAA CTTCTGGGCT CAATTGATCC CCTGCCTCAG 2640 CTCCCACAGT GCTGGGATTA CAGACGTGGG CCACCACTCC TGGCCTTATT TTCTATTGAT 2700 ATAGATTAAT TTGCTTTTTT GAATAAATGA AATCATACAG TATGCATTTT TTTTATGTCT 2760 GGTTTCTTTT GCACATGTAA TTTTTAAGTA ATTCATTTGT GTTATGTGTA TATAAGAGTT 2820 TGTTTTAAAA AAAAAATCTG GGCCGGGCAC GGTGGCTCAC ACCTGTAATC CCAGCACTTT 2880 GGGAGGCCGA GGCGGGTGGA TCACGAGGTC AGGAGATCGA GACTATCCTG GCTAACATGG 2940 CGAAACCCCA TCTCTACTAA AAATACAAAA ACAAAATTAG CCGAGCTTAG TGGCGGGTGT 3000 CTGTAGTCCC 3010
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