Tag | Content |
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EnhancerAtlas ID | HS180-31857 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr22:36814780-36816960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr22:36816599-36816609 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr22:36816599-36816609 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr22:36816599-36816609 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr22:36816599-36816609 | AACAGCTGTT | - | 6.02 | Zfx | MA0146.2 | chr22:36816890-36816904 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01080 | chr22:36815052-36816054 | Adrenal_Gland | SE_09195 | chr22:36815068-36816039 | CD14 | SE_23071 | chr22:36815208-36815913 | Colon_Crypt_1 | SE_23071 | chr22:36816162-36816817 | Colon_Crypt_1 | SE_23740 | chr22:36815198-36815895 | Colon_Crypt_2 | SE_23740 | chr22:36816245-36816671 | Colon_Crypt_2 | SE_24731 | chr22:36815495-36815926 | Colon_Crypt_3 | SE_24731 | chr22:36816226-36816782 | Colon_Crypt_3 | SE_27650 | chr22:36814561-36817422 | Fetal_Intestine | SE_28644 | chr22:36814534-36817532 | Fetal_Intestine_Large | SE_31378 | chr22:36814781-36815933 | Gastric | SE_31378 | chr22:36816180-36816888 | Gastric | SE_37504 | chr22:36814759-36817554 | HSMMtube | SE_40597 | chr22:36815120-36816847 | Left_Ventricle | SE_42094 | chr22:36814585-36816153 | Lung | SE_42094 | chr22:36816173-36816849 | Lung | SE_47757 | chr22:36815488-36815856 | Pancreas | SE_50050 | chr22:36814593-36816138 | Sigmoid_Colon | SE_50050 | chr22:36816153-36817226 | Sigmoid_Colon | SE_52340 | chr22:36814707-36816100 | Small_Intestine | SE_52340 | chr22:36816150-36816885 | Small_Intestine | SE_53283 | chr22:36814653-36816958 | Spleen | SE_58448 | chr22:36724049-36832686 | Ly1 | SE_62151 | chr22:36773097-36852649 | Toledo | SE_63127 | chr22:36801020-36866853 | Tonsil | SE_65459 | chr22:36815057-36816054 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036418 | chr22 | 36814698 | 36817466 |
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Enhancer Sequence | ATAGCGACTG GGTGTCACTA TGTTGCCTAC ATTGGTCTCA AACTCCTCGG TCTCCCAAAG 60 CGCTGGGATT GATGTAGGAG GTGGGACTCG ACTCTGGAGG TGGGGCTCAC ACATTGAACC 120 AAATCAAGGA CTAGCTAGGC TGGGCGCTGT GGCTCAAGCC TGTAATCCCA GCACTTTGGG 180 AGGCTGAGGC GGGTGGATCA CGAGGTCAGG AGTTCGAGAC CAGCCTGGCC AACCTGGTGA 240 ACCATCATCT CTACTGAAAA TAAAAAAATT AGCCAGGCAT GGTGACGGGT GCCTGTAGTC 300 CCAGCCTCTC GGGAGGCTGA GGCAGGAGAA TAGCTTGAAC TCGGGAGGCA GAGGTTGCAG 360 TGAGCCGAGA CCATACCACT GCACTTCAGC CTGGGTGACA GAGCGAGACT CTCTCTCAAA 420 AAAAAAAAAA AAAAAAAAAA GAGAAAAAGA AAAGGAAGAA CAGAAGAACA GAAGAGAAAG 480 GGCACCCCAC ACACATCCAT TCCTCTCTTC CTCCGTTAAA CCGGAGCCAG GGGCTGGGGC 540 TGGGTGTGTG TGCTCCTGCC TTCCCAGGCT CTTGCTTGTT TTCAAAGGAC CAGAGAAATG 600 TCTGGAGGAC TGCTGCTTCA GTCCACGTGA CCAGGATGAA AGTCATTAAC AAAAGGCCAA 660 TGTTTGGGGA AGAGCCTTTG CCCTCCTTTC AGGGCCTCAG CTGGGGCTCA GGGAGATAAG 720 GCGGGAGCAA AAATAAAACT GAAAATGTGT TTACTCTGAG ATGAAAGTGC ATTGCTAAAC 780 GCTAGCCGCG AGGACTTGTA TACAAAAACC ACATGTCTGG GGGTGTTCTG GAATGTCACA 840 AACTGCAATG GCAAGAAAAG GCAGCAGGCA GGACCAGGAC TCTGCTCCGT GGGAGCCCCC 900 TCTGGTGCCC TGGCTCTGTC ACCTCCTAGG GTCTGTGATC TCTCAAACCG GACCTCAGAC 960 AGCCTGAGCA GCCCACCCAG CCACGTGAGC CACCGTGCCC AGCCTGATTT CTTTCTTTCT 1020 TTTGTTTTCT TTCACTTTTT AAACAGAGAC CAGCAGGCCA GGTGCGGTGC CTCACGCCTA 1080 TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GTGGATCACC TGAGGTCAGG AGTTTGAGAC 1140 TAGCCTGGCC AAGATGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAT TAGCTGGGCG 1200 TGGTGGCGGG TGCCTGTAGT CCCAGCCACT CGGGAGGCTG AGCCGAGATC GCACCACTGC 1260 ACTCCAGCCT GGGAGACAGA ATGAGACTCC GCCTCAAAAA AAAAAAAAAA AATTAGCCTG 1320 GCGTGGTGGT GGGTGCCTAT AATCCCAGCT ACTCGAGAGT CTGGGGCAGG AGAATTGCTT 1380 GAACCCGGGA GGCAAAGGTT GCAGTGAGCT GAGATAGCGT CATTGCACTC CAGCCTGGGC 1440 AACAGAGCGA TACTCCGTCT CAAAAAAAAA AAAAAAAAAA GCCATGAGTG AGTTACTCTT 1500 GCGAGCAGCC CTCTCGAGCT GGAGTTTGAC TCCTGGAAGA TGGGATGCCA CTGTGACTGA 1560 GCAAACATAG GAATAGCTGT TCCACTAAAG TCTCACAAAG CCACTGGCCG GAGGAATTTC 1620 TCTAGGGACT CCCAGGAGCA GCTGAGGAAA CATGAAGGAG TGGACATTCC CAGAAGCCAA 1680 AGAAAAGTCG TTTGGTTACA GAGACTGGTG TCTGTGTTCT TCTAGAAAAC ATGGGCTCTG 1740 CTGAGATCAG GGAAGACTCT GACAGGAGCC ACCAGGCAGA ATCCTCCAGA CAGACTAGAA 1800 TGAGTACAAA GGAGAACAGA ACAGCTGTTG CTGGGCGTTT GGACTGAACA GACCTTTCTC 1860 ACGTGTTGTT TTTATTTATT TATTTGGAGA GAGTCTTGCT CTGTTGCCCA GGCTATAGTG 1920 CAGTGGTGAG AACTTGGTTC ACTGCAACTT CCACCTCCTG AGTTCAAGCT ATTCTCCTGC 1980 CTCAGCTTCC TGAGTAGCTG GAATTACAGG AGTGAGCTAC CATACCTGGC TAATTTTTGT 2040 ATTTTTAGCA GAGACGGGGT TTCAGCATGT TGGCCAGGCA GGTCTCAAGC TCCTGGCCTC 2100 AAGGGATCCA CCCGCCTCGG CCTCCCAAAG TGCTGGAATT ATAGGCATGA GCCACCACAC 2160 CCAGCCTGTT ATTATTTTTT 2180
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