Tag | Content |
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EnhancerAtlas ID | HS098-48124 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:30719130-30721510 |
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 | TCACCATGTT GGCCAGGCTG GTCTGGAAAA CTCCTGACCT CACGTGATCC GCCCCCTCGG 60 CCTCCCAAAG TGCTGGGATT ACGGGCGTGA GCCACCACAC CCAGCAAAAA AAAAAATTTG 120 TTTTTACTCA CCACTATACT GACAAGGAAC AGGTGATTTT AAACATCCCC TCCCACCTAC 180 ATTTTAGCTG GAACAATTCT CCAGAGGCAT GGGGGTAGAG TGGGGTGGTG AGTTCTAGGC 240 AGCAAGTTAA CAAATGACCC CTAAAGATAT TCATCTAGGC TCTAGGAGGC CCAAAATCAG 300 GCCCTGGCAG TTCCCCTGAC GCAAAACCAT GGCAAGAGTT CCGGGAGCAC CAAGGCAAGG 360 TCACAAAAGT GGCACGATGA CCCTACCCTG GGATGCAGCT CAGCCTGACC CAGCCCAACT 420 CAACCCAGCT ACCCTGGAGG CTGCTATGAG CTGAGCCGGG AGCTGGGAAA GGGCCCAGCA 480 TTCCTGTCCT TCTGCCAAAG CCGGCTTCTT AGGACCCCAG TGTTGTGGCT CCTCCTTTGG 540 TCTTGGTTTC TTTCCCACCA GATTATAACT CCACCAGAGT AGGACTTTAT CTATCTTGTG 600 TACTGCTCTA TTTTCAGTGC CTAGAACTGT GCCTGTCAAT CAATACAGGC TGCTGAAAAG 660 GCTAGAAATA CAGGATCGTT GATGTCATTA CTGTTACAGT GCTGTTCCCG TGGGAAGCAG 720 CCTGCATCTC TCTGTAGACA GCTCCAATGT CAGCCATTGG AGAATTTGAT GGAGATTGAA 780 GTCAAAACAT AATCATAGGG GAAAAATGCA CAACAAATAA AATATTTCCC CTTTTGTCCA 840 GACTTTTCAG ACACCCCGTA TTTACTGGAT GAGTTGATCT ACAAAGTGAA AGGCATAAAT 900 TAAAGGCTCT CTAATGTTTC TCCTCCTCTG AAACCCCATG ATTCAGCAGC GTCTCCCATG 960 TGTGCTCAAA AGTTGGACGT GCCTCCAGCC TACCCTCCAA AGCAGTTGCC ATAGGCTCTT 1020 TTCTTCCAAG GTTGGGAGGG ACAGTTCATT CCCCAAGAGG CCTCTCCAGG GGCGGAGGCG 1080 GGTGCTGGGG CTGGCCTGTC TGCAGCTCCC TGGCCCTACC CAGTGGGGAT CGCGTGTCAG 1140 TACTGGGGTT TGGTGGGCTG CCAAGGGGTG AGCCCTGAGG CGGTTTTCTG GGAAGGATAG 1200 ATGCCATGTG TGACTCAGAA CCAAGTTAGG GAAAAAACAA GCTCACTCAA TCTCTAGCAC 1260 CCTCTGCCTG GCCTGGCTTT GCCCATGAGC TCATAAAAGA GGAAGCTGGG CCGGCCAGAC 1320 AGTAGCTCTG CTTTCCCTCA TGTTTTCTCT CCACGTCTCA CGGATTCCCT AGAGTGTCTG 1380 GGCCTCAGGC CACCGTCATC CTAGCTCCTG GGCCCTGGCT CTTTTATGAC ACTTTCCCTT 1440 CCCAGACACT TGGTCATTTC TTTCCCCAGG TTGGGAATCC CACCTACCAT AGAAGGGGAA 1500 TTGCACACAA GGGGAGGTTG CAAATCTCTG TGTTCCTTGG CCCTGCTGAG GCCTCCACTG 1560 TCAGCCATGA CCATTTGGGT TTGTGCGTGT GACTGCTGTG TCTCTGACAC AGACCAAGTG 1620 GTGCTGACCC TGGGAGCCTG AATTAATAGA TTTCTTGAGA GCTGAGATTC TCTGGTTCAG 1680 GAAAGAAAAA GGGGGTACCA AATGACTGGG CAGCCGAGCC ACCCTCAGGG CTGCAATATT 1740 CCAGTTGGGA CCAACTTACC TAGTACTTTT GGCATTCAGA ACAGTTCACT ACCAAAAAGG 1800 CACATTTTAT TTTAGTGAAA ATGGGACAAT CATGGGCCAT AAAGAACCTT CCTAACTATT 1860 GTTCCTCCGG TTCACCTCCT ATACCCCCCA GGGCTTTCTT GTTCAAAGAC AGACTTGACC 1920 ATGTCCATGC CTGCTTCAGT AAGTTCAGTG GCTCCAAACT CTCTGAGTTC CCAACCCAAA 1980 TCCAGGCACC TTGCAGGCTT TCTCTTTCAA CACCCCCATT GCTTCTTGAT GTTGTGCATC 2040 TCTAATTTTG TCCTTTTTCT CACACATGCC AAACTCTTAC CCATTGGACC CTATAACCGT 2100 TCTATTTCTT TTCCTTTTTC CTCCCTATTC TCCTGGGAAA AAACCACTCC TGAACCTGCC 2160 ATCCAGAATT AGTTCATCTA CATTGTATAC AAATCTCTCA AAGCATCACA CACACGATAT 2220 TATAGTCATT TGTCTATCTT TTTGATTGCC AGGAGAGGCA CGTGCCATTG AGATGCAGCC 2280 GTCTTAATAC TGGTAACCTC TTGACAAGGC CTAAAATTAT TATTAAATTG TCACCATTAA 2340 AAAAAAAATC AGTGGCCAGG CACGGTGTCT CATTCCTGTA 2380
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