Tag | Content |
---|
EnhancerAtlas ID | HS177-24499 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chrX:40034090-40036250 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chrX:40036088-40036098 | GCACGTGACC | - | 6.02 | RREB1 | MA0073.1 | chrX:40034411-40034431 | GGGGGTGGGGTGGGGCGGGG | - | 6.18 | RREB1 | MA0073.1 | chrX:40036206-40036226 | CCCCACCCCACCCCCTACCT | + | 7.21 | RREB1 | MA0073.1 | chrX:40036201-40036221 | CCCCACCCCACCCCACCCCC | + | 7.67 | RREB1 | MA0073.1 | chrX:40034406-40034426 | GGGCTGGGGGTGGGGTGGGG | - | 7.6 | Zfx | MA0146.2 | chrX:40034513-40034527 | CAGGCCCCGGCTGG | - | 6.11 | Zfx | MA0146.2 | chrX:40035598-40035612 | CCGGCCTCGGCCTC | + | 6.28 |
|
| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01309 | chrX:40032735-40036795 | Adrenal_Gland | SE_10489 | chrX:40028005-40037299 | CD19_Primary | SE_12441 | chrX:40028224-40037012 | CD3 | SE_13187 | chrX:40029966-40036585 | CD34_Primary_RO01480 | SE_13805 | chrX:40028268-40037234 | CD34_Primary_RO01536 | SE_14344 | chrX:40029761-40037049 | CD34_Primary_RO01549 | SE_15054 | chrX:40026645-40037112 | CD4_Memory_Primary_7pool | SE_26729 | chrX:40030073-40036950 | Esophagus | SE_31755 | chrX:40030098-40036960 | Gastric | SE_32909 | chrX:40033848-40036162 | H1 | SE_34319 | chrX:40025113-40037081 | HCT-116 | SE_39958 | chrX:40029745-40037040 | K562 | SE_41477 | chrX:40032964-40037003 | Left_Ventricle | SE_42747 | chrX:40030207-40037520 | Lung | SE_49191 | chrX:40030107-40036942 | Right_Atrium | SE_52969 | chrX:40029971-40037549 | Small_Intestine | SE_54123 | chrX:40032886-40037231 | Spleen | SE_55438 | chrX:40032592-40037070 | Thymus | SE_56999 | chrX:40033538-40036784 | VACO_400 | SE_57737 | chrX:40034438-40036171 | VACO_503 | SE_59437 | chrX:40011613-40049393 | Ly3 | SE_60054 | chrX:40006843-40037107 | Ly4 | SE_61279 | chrX:40005072-40049257 | HBL1 | SE_61737 | chrX:40005446-40039231 | Toledo | SE_62904 | chrX:40005186-40037678 | Tonsil | SE_65537 | chrX:40032894-40036865 | Pancreatic_islets | SE_66639 | chrX:40032989-40035974 | Jurkat | SE_68820 | chrX:40032750-40036863 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 40034377 | 40034649 | chrX | 40034694 | 40035505 |
|
Enhancer Sequence | AGTTTCTCAC AGTATTTCTA ATTGATTCAA CGTGTATTAG ATTGAAACAA AAATGATCTT 60 GGTTGGAATA TACACGGGCA ACCTGTATTT AGATGGGGTA AGTTCCTGCA GCTATCTGAC 120 CACATTTGTC TGGTCCCTCT GAGAATCCAC GTTTTCTAGC CCGAGAAGGG GCAGGCGGCC 180 CTCATGGCGC CTCCTTCGGC GGTTTCCTGG CGAAGCGCCC ATCCTCCCCA AGCACCAGGA 240 ACGGAGGCCG TCCATATTAA TACTCGCGGG CAGCCTGTTC TGACCTATAC TGTCATTTTT 300 TCCATCGGTC GGGATCGGGC TGGGGGTGGG GTGGGGCGGG GGCTCTCCTC CGAGGGGCTC 360 AGCACGGATC GTTGGGTTTT CCCCGGCGAA CTTAACACGG AGGCAAAAGG GGCAGATGGA 420 AACCAGGCCC CGGCTGGCCC CGCGCGCGTA AGCGCGGCAC TCAGCAGCTC GACGCAAAGC 480 CAGGGCTGGA TTTTCGCGGC CCGGGCCCGG CGGCCGCCCA GCGCCCGCGC GATCCTCTCT 540 CCTTCGGGTT GAGCAAACGT GGTCGCCTAA TTCCGCCCGG GAGACAGCAG CTGTGCGGCG 600 AGAGGGGGAG AAAAAATATC GCAACTTTTC CAACAGAAAG TGTGTGCGCA CACGAGAGGT 660 GAAGGCCCAC CCCGATTCTG TGCACGTATC GACACAGCAT CTAATCAGTG TCACTGCCAG 720 GAATACGCTT CCGCGGCGGG CGACACCGCC GCCCTCGCCA ACCTGCAGGA GGGAGGGGGG 780 ATGCAAATGG CGTCTCGCGT CGTCCTAGAC TCCGCGCAGC ACCCGCTACC GCGACTCCAA 840 GCAGACGTTG CAGCAAACTG GGGTGCAGCG TCTGGGGACG CGAACGCGCA GGCGGCCCGA 900 GCGGTCGCAG GGAAGAGGAA CTAGCACCAC TCCCCGCTAC GAGACCGTTC CCCGCCCCCA 960 CCTCCGGAAG AGCCGCCCTT ACTCGACTGG GGTGAGGGGC GGGAAACTTT GCAAGAAGAC 1020 TGTTCCGCGC CTTCCCCGCG TGGCACCTCA GAAGAACGTG GGTGGGTTTC CCGTCCGAGG 1080 CCAGACCACG CTACCCTACT TTTCCAGGTT TCGGACCTGA ACCTCGTGGA CTACGGGAGG 1140 GAGAGTACAT TTCGGGCCAC TGCGGGGGGC GGAGGGACAC CAAAGACAGG CGTCTTCAAG 1200 GGTTCTGGCA GATGGCCAAG TTTGTGTCCT TTCCCTCCCA CGCTAGAGTA GCGCACGCCA 1260 CTTTGGGGAA GCGTGAGACC GTTCACCACC GGCCACGAGG CCACCAATGT CTTCCAGGTG 1320 GGGCCGATGG TTTGTCTGCA GCACTCCCTT CCGCCTTGCG GTCCTCGCCT GGCTCCCACA 1380 GTCCTGGGGA GCCCCCAGAG CTAGCCCGCG TCTTCCCTCG CCCGCTCTTC CGGGGGAAAG 1440 GGAGGCTGTT TGTGTGGTGT GTAGCCCCGC TCCGGCTTGC ACCCCCGCGA GCCACCTCGC 1500 AGCCCTCCCC GGCCTCGGCC TCACGGATCC CCTCCCGGAG TAGCCCCGCG GGCCCCCCCG 1560 CCATGCGTAA TGGGGCGCCC CTGGGACGCA GGCGGGGATG GCGGTTCCGG TCGTTCCGGG 1620 ATTTGCGTGC AAGAAGAAAA CAAGGCCGGC GACTACAAGA GCGGCGACTC CATTCTTGGG 1680 GTTCAGACGC CCTCGCAGCC TCCGCGTCGG TTCCGCTCTC GCCCCGGGAG CCCGCTTCCG 1740 TGTCCCTGCC CCCGCCCCCC AACGATTCCT CGTCCGGCCC GTGCCGCACC ACGCGGAGCT 1800 CCGCGCGCCC TGGCTCCCAC ACCGGTCCCT CCATAACTCG CGCTCCTCCC TCGCTCCGGG 1860 CTCGGGGAGC CGCTCGCTCC CAGCGCCCAG AGTCAGCCGG TTCCACCTTC GGCTGCGAGA 1920 GCCGCCGCCC CGCGCCACCC CCGCCCGGCC CGGCCCTTGT CCCAGCCCGG CTCCCCCGCC 1980 AGCTGCGCCG CCACCGCCGC ACGTGACCCG CCCCCGTCGC GGCTTCCGCT GAGCTGCCTG 2040 TTCCGGGGCA CAAACAATTT TTGCTCTGAC GCGGGGTCTC TCGGGGGCCC TGGCGTCCTC 2100 TACTCCCTGC TCCCCACCCC ACCCCACCCC CTACCTTCCG GGTAGGAGAA CTCAAAACAA 2160
|