Tag | Content |
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EnhancerAtlas ID | HS052-32358 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:30718950-30721520 |
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 | AACTCCGTCT TAAAAAAAAA GAAAGTCTTA CTCTGTCGTC CAGGCTGGAG TGCAGTGGCA 60 CAATCTCGGC TCACTGCAAC CTCTGCCTCC CGGGTTCAGG CGATTCTCCT GCTTCAGCCT 120 CCCGAGTAGC GCATGCCACC ATGCCCGGCT AATTTTTGTA TTTTTGGTAG AGATAAGGTT 180 TCACCATGTT GGCCAGGCTG GTCTGGAAAA CTCCTGACCT CACGTGATCC GCCCCCTCGG 240 CCTCCCAAAG TGCTGGGATT ACGGGCGTGA GCCACCACAC CCAGCAAAAA AAAAAATTTG 300 TTTTTACTCA CCACTATACT GACAAGGAAC AGGTGATTTT AAACATCCCC TCCCACCTAC 360 ATTTTAGCTG GAACAATTCT CCAGAGGCAT GGGGGTAGAG TGGGGTGGTG AGTTCTAGGC 420 AGCAAGTTAA CAAATGACCC CTAAAGATAT TCATCTAGGC TCTAGGAGGC CCAAAATCAG 480 GCCCTGGCAG TTCCCCTGAC GCAAAACCAT GGCAAGAGTT CCGGGAGCAC CAAGGCAAGG 540 TCACAAAAGT GGCACGATGA CCCTACCCTG GGATGCAGCT CAGCCTGACC CAGCCCAACT 600 CAACCCAGCT ACCCTGGAGG CTGCTATGAG CTGAGCCGGG AGCTGGGAAA GGGCCCAGCA 660 TTCCTGTCCT TCTGCCAAAG CCGGCTTCTT AGGACCCCAG TGTTGTGGCT CCTCCTTTGG 720 TCTTGGTTTC TTTCCCACCA GATTATAACT CCACCAGAGT AGGACTTTAT CTATCTTGTG 780 TACTGCTCTA TTTTCAGTGC CTAGAACTGT GCCTGTCAAT CAATACAGGC TGCTGAAAAG 840 GCTAGAAATA CAGGATCGTT GATGTCATTA CTGTTACAGT GCTGTTCCCG TGGGAAGCAG 900 CCTGCATCTC TCTGTAGACA GCTCCAATGT CAGCCATTGG AGAATTTGAT GGAGATTGAA 960 GTCAAAACAT AATCATAGGG GAAAAATGCA CAACAAATAA AATATTTCCC CTTTTGTCCA 1020 GACTTTTCAG ACACCCCGTA TTTACTGGAT GAGTTGATCT ACAAAGTGAA AGGCATAAAT 1080 TAAAGGCTCT CTAATGTTTC TCCTCCTCTG AAACCCCATG ATTCAGCAGC GTCTCCCATG 1140 TGTGCTCAAA AGTTGGACGT GCCTCCAGCC TACCCTCCAA AGCAGTTGCC ATAGGCTCTT 1200 TTCTTCCAAG GTTGGGAGGG ACAGTTCATT CCCCAAGAGG CCTCTCCAGG GGCGGAGGCG 1260 GGTGCTGGGG CTGGCCTGTC TGCAGCTCCC TGGCCCTACC CAGTGGGGAT CGCGTGTCAG 1320 TACTGGGGTT TGGTGGGCTG CCAAGGGGTG AGCCCTGAGG CGGTTTTCTG GGAAGGATAG 1380 ATGCCATGTG TGACTCAGAA CCAAGTTAGG GAAAAAACAA GCTCACTCAA TCTCTAGCAC 1440 CCTCTGCCTG GCCTGGCTTT GCCCATGAGC TCATAAAAGA GGAAGCTGGG CCGGCCAGAC 1500 AGTAGCTCTG CTTTCCCTCA TGTTTTCTCT CCACGTCTCA CGGATTCCCT AGAGTGTCTG 1560 GGCCTCAGGC CACCGTCATC CTAGCTCCTG GGCCCTGGCT CTTTTATGAC ACTTTCCCTT 1620 CCCAGACACT TGGTCATTTC TTTCCCCAGG TTGGGAATCC CACCTACCAT AGAAGGGGAA 1680 TTGCACACAA GGGGAGGTTG CAAATCTCTG TGTTCCTTGG CCCTGCTGAG GCCTCCACTG 1740 TCAGCCATGA CCATTTGGGT TTGTGCGTGT GACTGCTGTG TCTCTGACAC AGACCAAGTG 1800 GTGCTGACCC TGGGAGCCTG AATTAATAGA TTTCTTGAGA GCTGAGATTC TCTGGTTCAG 1860 GAAAGAAAAA GGGGGTACCA AATGACTGGG CAGCCGAGCC ACCCTCAGGG CTGCAATATT 1920 CCAGTTGGGA CCAACTTACC TAGTACTTTT GGCATTCAGA ACAGTTCACT ACCAAAAAGG 1980 CACATTTTAT TTTAGTGAAA ATGGGACAAT CATGGGCCAT AAAGAACCTT CCTAACTATT 2040 GTTCCTCCGG TTCACCTCCT ATACCCCCCA GGGCTTTCTT GTTCAAAGAC AGACTTGACC 2100 ATGTCCATGC CTGCTTCAGT AAGTTCAGTG GCTCCAAACT CTCTGAGTTC CCAACCCAAA 2160 TCCAGGCACC TTGCAGGCTT TCTCTTTCAA CACCCCCATT GCTTCTTGAT GTTGTGCATC 2220 TCTAATTTTG TCCTTTTTCT CACACATGCC AAACTCTTAC CCATTGGACC CTATAACCGT 2280 TCTATTTCTT TTCCTTTTTC CTCCCTATTC TCCTGGGAAA AAACCACTCC TGAACCTGCC 2340 ATCCAGAATT AGTTCATCTA CATTGTATAC AAATCTCTCA AAGCATCACA CACACGATAT 2400 TATAGTCATT TGTCTATCTT TTTGATTGCC AGGAGAGGCA CGTGCCATTG AGATGCAGCC 2460 GTCTTAATAC TGGTAACCTC TTGACAAGGC CTAAAATTAT TATTAAATTG TCACCATTAA 2520 AAAAAAAATC AGTGGCCAGG CACGGTGTCT CATTCCTGTA ATCCCAGCAC 2570
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