Tag | Content |
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EnhancerAtlas ID | HS138-00267 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:16506920-16509390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr1:16508229-16508242 | CTACTTCCGGCTA | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr1:16508479-16508497 | GGGAGGAAGGAAGCAGAG | + | 6.42 | LMX1B | MA0703.2 | chr1:16507192-16507203 | ATTTTAATTAA | + | 6.62 | Lhx3 | MA0135.1 | chr1:16507206-16507219 | AAATTAATTATTT | + | 6.78 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16507977-16509332 | Colon_Crypt_1 | SE_24743 | chr1:16508183-16508861 | Colon_Crypt_3 | SE_26540 | chr1:16504790-16512175 | Esophagus | SE_28102 | chr1:16507825-16509373 | Fetal_Intestine | SE_29455 | chr1:16507734-16509371 | Fetal_Intestine_Large | SE_31527 | chr1:16507486-16509710 | Gastric | SE_34268 | chr1:16506936-16512113 | HCT-116 | SE_34628 | chr1:16506549-16512234 | HeLa | SE_36144 | chr1:16507720-16509431 | HMEC | SE_38062 | chr1:16507125-16509874 | HUVEC | SE_40833 | chr1:16507342-16509479 | Left_Ventricle | SE_44998 | chr1:16507356-16509449 | NHLF | SE_46140 | chr1:16507347-16510631 | Osteoblasts | SE_47009 | chr1:16507488-16507895 | Ovary | SE_47009 | chr1:16508039-16509386 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16507579-16507933 | Pancreas | SE_47539 | chr1:16507961-16508560 | Pancreas | SE_47539 | chr1:16508587-16509159 | Pancreas | SE_48744 | chr1:16507441-16509527 | Right_Atrium | SE_50427 | chr1:16507395-16509522 | Sigmoid_Colon | SE_52536 | chr1:16507445-16509419 | Small_Intestine | SE_56795 | chr1:16506234-16507286 | VACO_400 | SE_56795 | chr1:16507333-16512008 | VACO_400 | SE_57357 | chr1:16508000-16508578 | VACO_503 | SE_57357 | chr1:16508592-16509318 | VACO_503 | SE_57939 | chr1:16507977-16509011 | VACO_9m | SE_64726 | chr1:16507942-16511421 | NHEK | SE_65472 | chr1:16507356-16509554 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16508086 | 16509162 | chr1 | 16508402 | 16508642 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | CATCTCAAAA AAAAAAAAAA AAAAGATTTA CTGGTCCCCT GTTGTGTTTT AGGCATGAGT 60 CAGATGCTGT GGATATAGCA ATGAACACAG CAGACAAAGG TCTCTGCCTC TGTGAAACTG 120 ACATTGGAGA ACAGCAGTCT AGAAGAACTT GCTGTGGATG GAATGATGAA TGGATAGAAA 180 CGTTTTACAT CTGCTCCGCA CTGGCCGCAC GCGGCTACTG AGCACTTGAG ATGCGTCTGG 240 TGCACCTGAA GAGCTGACTT TAATTTTATT TCATTTTAAT TAATTTAAAT TAATTATTTG 300 TTTATTTGAG ACAGAGTCTC GCTCTGTCAC TCAGGCTGGA GTACGGTGGC GCAATCACAG 360 CTCACTGCAA CCTCTGCCTT CTGGGCTCAA GCCAGCCTCC TACCTCAGCC TCCTGAGTAG 420 CCAGGACTAC AGGTGTACAC CACCACACCC AGCTAATTTT TTGCGTGCTT TTTGTAGAGA 480 TGGGGTTTCA CCATGTTGCC TAGTCTGGTC TCGAACTCCT GACCTCAAGA GATCCACCCA 540 CCTTGGATCC CAAAATGCTG GGATTACAGG CATGAGCTAC TGCGCCCGGC CTCTAGATTT 600 AAATAGTACC TACCGAACTG GCCAGTGCAG CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA 660 GAGCTGGGCC TGGCTGTGTG TTATTCACGT TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC 720 CTCTGGCAGC AGAATCACCT GGGAAGCCAA AACTTCAGAT CCCTGGGATC CCAGACCCAC 780 TGAATCAGAA TCTCCGAGGC CAGGGCTTGG GCGTCTGCCC GTTCACCACA CACCCCAGCT 840 GATTCTGATG CACATGAGGT CAAGTTTGAA ACCCACCCCA CTGCCCTAGT TGTTCAAGAC 900 TCCCAGCGCT GGCTGGATGC AAAGTCTTAT GCCTGTAATC CCAGCTCTTT TGGGAGGCCA 960 AGGCGGGCAG ATCACTTGAG GTCAGGAGTT CGAGACCAGC CGGGCCTACA GAGTGAAACC 1020 CCGTCTCTAC TAAAAATACA AAAATTAGCT AGGTGTGGTG GTGGGCGCCT GTAATCCCAG 1080 GAGGTGGAGG TTGCAGTGAG CCGAGATCGC GCCGCTGCAC TGCATCCTGG GCAACAGAGC 1140 GGGACTCCGT CTCAAAAAAA AAAAAAGACT CCCGGCCAGG AAGAGAGCTT GAATGAAGTC 1200 TGACCTGCAC CAGGCCTTCT GGGCCCAGAC CAGGCCTGCT TAGGGGCATG TGCCCTGCTC 1260 AGAACTTCCC CATCCCAGCT AACCCAGAAG ATAGCTGGGA TGAAGATAGC TACTTCCGGC 1320 TACCAGCCCA TGATTCTTTG CCAGCCTGCA CTGTTCCCTG AAGAGCAAAA AGACTTGGAA 1380 TTTCCCTGCT CTATCCAGAG GGGCTGGGAT GAGGGGTCCT GAGTTCCCTT ATCCCATGTC 1440 CTACCAACCT CTGGAGCTCT CCAGTCAGCC AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC 1500 AATGGGAGGG AGAGGCTTGG CCCAGCACCC CACCCCACAG ATCAGCCTGG TCCGGCAAGG 1560 GGAGGAAGGA AGCAGAGGCA GCCTGGGCCA GCGGACACAG GGTTGGGGGT GACACAGGCC 1620 TCAGGAATTT GAAAACAAAC ACTTCGCCAG GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG 1680 CCCGGGCGGG CCCAGGTCCC TCCCTTTCAG GGCAGGGGTG AATCCCAGTG CTGCTGACCA 1740 TGGCCCCCGG CTGGACCCAG TGCTCGGGGA GTTTCCACTC CGCTGGTGGG ATGGGAAGGT 1800 CATGGGAGGT GTGGGGGGAT CCAGGCTCTG TCCAGATACG GGAGCATCCT GGCTGGGGTG 1860 AGGACAGGAA GGGACAAAGA GCTGGGAAAG CCACGAGACC CCAGGAGAAG GCTCAGCAGC 1920 AACAGGATGC CGCCTCAAGC ATTTATTGAG CACCCATGGT ATTCCAAAAA CTGAGAATAT 1980 AAGCACTGCC TAGCTGGGGA GATCAGGGGA AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA 2040 GGTGGCATTG AACTGAGCCC TGAAAGGTAA ACTAGGACCG GGGAGGACAG AATCTTACAA 2100 GTCTCCCCCC TTCACACTCC CAGAGCCGGC GCTCAGTGAG TGCATGAGTG AGTAAGCGGC 2160 TGACCAGCGA CTATGCAGCA TGAATGAATG ACAGACTGAA TGACATGAAG CCTGGAGTCT 2220 CAAGGCCGAG ACTGCAAAAG AAGAGTCCAT CCTCCTATCC CCTCTGCTCT GAACTCTCTT 2280 CATGATCCTG AAGGTGCTTG GTACCTGGAG ACTACGGAGC CAGCCTGCCG GGGTTCTAGT 2340 CTGAACTCAG TCACTTCCCA GCTGTGTAAC TTTGGACAAG TTACTTAACC TCTCTGTGCC 2400 TCTGGTCCCT TCTCTGTAAA GTGTAGTCAT CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT 2460 CCCAGCACTT 2470
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