Tag | Content |
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EnhancerAtlas ID | HS105-68459 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:30718940-30721590 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr6:30721386-30721396 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr6:30721386-30721396 | GGCACGTGCC | - | 6.02 | STAT3 | MA0144.2 | chr6:30720314-30720325 | TTTCTGGGAAG | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01128 | chr6:30718864-30721264 | Adrenal_Gland | SE_01961 | chr6:30718974-30721597 | Aorta | SE_02278 | chr6:30718957-30723368 | Astrocytes | SE_24166 | chr6:30719301-30719700 | Colon_Crypt_2 | SE_25936 | chr6:30718906-30721941 | Duodenum_Smooth_Muscle | SE_31499 | chr6:30718792-30721261 | Gastric | SE_33790 | chr6:30719130-30721503 | HCC1954 | SE_34639 | chr6:30714361-30721671 | HeLa | SE_35985 | chr6:30718949-30723056 | HMEC | SE_37002 | chr6:30718639-30723618 | HSMMtube | SE_37990 | chr6:30718946-30722557 | HUVEC | SE_38900 | chr6:30719048-30721593 | IMR90 | SE_40867 | chr6:30719094-30721787 | Left_Ventricle | SE_42338 | chr6:30719035-30721602 | Lung | SE_46281 | chr6:30714983-30724044 | Osteoblasts | SE_47616 | chr6:30719245-30719791 | Pancreas | SE_47616 | chr6:30720011-30721100 | Pancreas | SE_48770 | chr6:30719116-30721503 | Right_Atrium | SE_49781 | chr6:30719237-30719949 | Right_Ventricle | SE_49781 | chr6:30719998-30721223 | Right_Ventricle | SE_51867 | chr6:30718943-30722524 | Skeletal_Muscle_Myoblast | SE_56270 | chr6:30719019-30720319 | u87 | SE_56270 | chr6:30720362-30721540 | u87 | SE_56775 | chr6:30718899-30721312 | VACO_400 | SE_57692 | chr6:30720321-30720916 | VACO_503 | SE_63673 | chr6:30718946-30722621 | HSMM | SE_64291 | chr6:30719060-30721623 | NHEK | SE_67519 | chr6:30719019-30720319 | u87 | SE_67519 | chr6:30720362-30721540 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 30719493 | 30720797 | chr6 | 30719490 | 30721457 | chr6 | 30720004 | 30720713 | chr6 | 30719576 | 30719814 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I030746 | chr6 | 30714432 | 30723976 |
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Enhancer Sequence | ACGAGAGTGA AACTCCGTCT TAAAAAAAAA GAAAGTCTTA CTCTGTCGTC CAGGCTGGAG 60 TGCAGTGGCA CAATCTCGGC TCACTGCAAC CTCTGCCTCC CGGGTTCAGG CGATTCTCCT 120 GCTTCAGCCT CCCGAGTAGC GCATGCCACC ATGCCCGGCT AATTTTTGTA TTTTTGGTAG 180 AGATAAGGTT TCACCATGTT GGCCAGGCTG GTCTGGAAAA CTCCTGACCT CACGTGATCC 240 GCCCCCTCGG CCTCCCAAAG TGCTGGGATT ACGGGCGTGA GCCACCACAC CCAGCAAAAA 300 AAAAAATTTG TTTTTACTCA CCACTATACT GACAAGGAAC AGGTGATTTT AAACATCCCC 360 TCCCACCTAC ATTTTAGCTG GAACAATTCT CCAGAGGCAT GGGGGTAGAG TGGGGTGGTG 420 AGTTCTAGGC AGCAAGTTAA CAAATGACCC CTAAAGATAT TCATCTAGGC TCTAGGAGGC 480 CCAAAATCAG GCCCTGGCAG TTCCCCTGAC GCAAAACCAT GGCAAGAGTT CCGGGAGCAC 540 CAAGGCAAGG TCACAAAAGT GGCACGATGA CCCTACCCTG GGATGCAGCT CAGCCTGACC 600 CAGCCCAACT CAACCCAGCT ACCCTGGAGG CTGCTATGAG CTGAGCCGGG AGCTGGGAAA 660 GGGCCCAGCA TTCCTGTCCT TCTGCCAAAG CCGGCTTCTT AGGACCCCAG TGTTGTGGCT 720 CCTCCTTTGG TCTTGGTTTC TTTCCCACCA GATTATAACT CCACCAGAGT AGGACTTTAT 780 CTATCTTGTG TACTGCTCTA TTTTCAGTGC CTAGAACTGT GCCTGTCAAT CAATACAGGC 840 TGCTGAAAAG GCTAGAAATA CAGGATCGTT GATGTCATTA CTGTTACAGT GCTGTTCCCG 900 TGGGAAGCAG CCTGCATCTC TCTGTAGACA GCTCCAATGT CAGCCATTGG AGAATTTGAT 960 GGAGATTGAA GTCAAAACAT AATCATAGGG GAAAAATGCA CAACAAATAA AATATTTCCC 1020 CTTTTGTCCA GACTTTTCAG ACACCCCGTA TTTACTGGAT GAGTTGATCT ACAAAGTGAA 1080 AGGCATAAAT TAAAGGCTCT CTAATGTTTC TCCTCCTCTG AAACCCCATG ATTCAGCAGC 1140 GTCTCCCATG TGTGCTCAAA AGTTGGACGT GCCTCCAGCC TACCCTCCAA AGCAGTTGCC 1200 ATAGGCTCTT TTCTTCCAAG GTTGGGAGGG ACAGTTCATT CCCCAAGAGG CCTCTCCAGG 1260 GGCGGAGGCG GGTGCTGGGG CTGGCCTGTC TGCAGCTCCC TGGCCCTACC CAGTGGGGAT 1320 CGCGTGTCAG TACTGGGGTT TGGTGGGCTG CCAAGGGGTG AGCCCTGAGG CGGTTTTCTG 1380 GGAAGGATAG ATGCCATGTG TGACTCAGAA CCAAGTTAGG GAAAAAACAA GCTCACTCAA 1440 TCTCTAGCAC CCTCTGCCTG GCCTGGCTTT GCCCATGAGC TCATAAAAGA GGAAGCTGGG 1500 CCGGCCAGAC AGTAGCTCTG CTTTCCCTCA TGTTTTCTCT CCACGTCTCA CGGATTCCCT 1560 AGAGTGTCTG GGCCTCAGGC CACCGTCATC CTAGCTCCTG GGCCCTGGCT CTTTTATGAC 1620 ACTTTCCCTT CCCAGACACT TGGTCATTTC TTTCCCCAGG TTGGGAATCC CACCTACCAT 1680 AGAAGGGGAA TTGCACACAA GGGGAGGTTG CAAATCTCTG TGTTCCTTGG CCCTGCTGAG 1740 GCCTCCACTG TCAGCCATGA CCATTTGGGT TTGTGCGTGT GACTGCTGTG TCTCTGACAC 1800 AGACCAAGTG GTGCTGACCC TGGGAGCCTG AATTAATAGA TTTCTTGAGA GCTGAGATTC 1860 TCTGGTTCAG GAAAGAAAAA GGGGGTACCA AATGACTGGG CAGCCGAGCC ACCCTCAGGG 1920 CTGCAATATT CCAGTTGGGA CCAACTTACC TAGTACTTTT GGCATTCAGA ACAGTTCACT 1980 ACCAAAAAGG CACATTTTAT TTTAGTGAAA ATGGGACAAT CATGGGCCAT AAAGAACCTT 2040 CCTAACTATT GTTCCTCCGG TTCACCTCCT ATACCCCCCA GGGCTTTCTT GTTCAAAGAC 2100 AGACTTGACC ATGTCCATGC CTGCTTCAGT AAGTTCAGTG GCTCCAAACT CTCTGAGTTC 2160 CCAACCCAAA TCCAGGCACC TTGCAGGCTT TCTCTTTCAA CACCCCCATT GCTTCTTGAT 2220 GTTGTGCATC TCTAATTTTG TCCTTTTTCT CACACATGCC AAACTCTTAC CCATTGGACC 2280 CTATAACCGT TCTATTTCTT TTCCTTTTTC CTCCCTATTC TCCTGGGAAA AAACCACTCC 2340 TGAACCTGCC ATCCAGAATT AGTTCATCTA CATTGTATAC AAATCTCTCA AAGCATCACA 2400 CACACGATAT TATAGTCATT TGTCTATCTT TTTGATTGCC AGGAGAGGCA CGTGCCATTG 2460 AGATGCAGCC GTCTTAATAC TGGTAACCTC TTGACAAGGC CTAAAATTAT TATTAAATTG 2520 TCACCATTAA AAAAAAAATC AGTGGCCAGG CACGGTGTCT CATTCCTGTA ATCCCAGCAC 2580 TTTGGGAGGC CGAGGTGGGC AAATCACCTG AGGTCAGGAG TTCGAGACCA GCCTGGCCAA 2640 CATGGTGAAA 2650
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