Tag | Content |
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EnhancerAtlas ID | HS111-04769 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr8:103802480-103804080 |
| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00329 | chr8:103798644-103804555 | Adipose_Nuclei | SE_00996 | chr8:103799522-103802677 | Adrenal_Gland | SE_00996 | chr8:103802759-103804065 | Adrenal_Gland | SE_01658 | chr8:103799617-103802647 | Aorta | SE_01658 | chr8:103802773-103803934 | Aorta | SE_26196 | chr8:103799641-103804464 | Duodenum_Smooth_Muscle | SE_27892 | chr8:103799762-103804205 | Fetal_Intestine | SE_28869 | chr8:103799804-103804295 | Fetal_Intestine_Large | SE_29616 | chr8:103799629-103804350 | Fetal_Muscle | SE_33791 | chr8:103799733-103803410 | HCC1954 | SE_34364 | chr8:103799752-103804222 | HCT-116 | SE_34740 | chr8:103799639-103808420 | HeLa | SE_37113 | chr8:103798461-103804394 | HSMMtube | SE_38251 | chr8:103799731-103804144 | HUVEC | SE_40837 | chr8:103799527-103804337 | Left_Ventricle | SE_42299 | chr8:103799542-103804376 | Lung | SE_44446 | chr8:103799700-103804309 | NHDF-Ad | SE_46287 | chr8:103799658-103804296 | Osteoblasts | SE_47342 | chr8:103799467-103805555 | Panc1 | SE_47635 | chr8:103802839-103803897 | Pancreas | SE_48146 | chr8:103799558-103804336 | Psoas_Muscle | SE_48645 | chr8:103798830-103804197 | Right_Atrium | SE_51194 | chr8:103799310-103804585 | Skeletal_Muscle | SE_51881 | chr8:103799734-103804314 | Skeletal_Muscle_Myoblast | SE_53417 | chr8:103796628-103804354 | Spleen | SE_54737 | chr8:103799409-103804612 | Stomach_Smooth_Muscle | SE_55530 | chr8:103802721-103803361 | Thymus | SE_55530 | chr8:103803443-103804173 | Thymus | SE_56070 | chr8:103799574-103804423 | u87 | SE_62939 | chr8:103793900-103843923 | Tonsil | SE_63674 | chr8:103799720-103804328 | HSMM | SE_65413 | chr8:103800556-103805167 | Pancreatic_islets | SE_67599 | chr8:103799574-103804423 | u87 | SE_68638 | chr8:103800188-103823262 | TC71 |
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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 |
GH08I102786 | chr8 | 103798917 | 103804339 |
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Enhancer Sequence | TAGAGACAGG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA ACTCCTGGCC TCAAGTGATC 60 CGCCTGCCTC AGCCTCCCAA AGTGTTGGGA TTACAGGCAT GAGCCACCTC ACCCAGCCGC 120 AAACATTTCT TAAACTAAAC TTTGTATTAA CTACATATTA CATAGTTCCT TATTGTAATA 180 AAATCTCCAG TGGCTAATTT GTTTTCTGTG CTTTTCTTTC TGTATTTTGT TACCCATATG 240 TGTTTTGGAA ATGTCCTGCT AGCGTATGGG AGACTACTCT ATTCTTATCT AATTATCAAT 300 GCTGTTGAAG GAAAATATCC TTTTACCTTT CTCTCCTGTT CCTTTTAAGA AAAACCCAAG 360 CACGAGCCTG TACTCTGTTT CCCCTGGAAA AGGAAGCTGC TAGGTGGGTC CCAGTGTTTT 420 TGGGAGGGTG GCTCCTGGTG AGTGACAGAC ACCCCTGGTG TACGCAGAGT CTTAAATGTC 480 TGCTCTGGAC TTTGAGTATG TGAGGCCAGA GGCCCAATTC TACAGGCTGG GCCAGAGGAG 540 GGCGTTTTTG GATGTTTTTA GGGCTGTGAG AATGTGTTCC CTTTATTTGT GCCTCCTTCT 600 GCTTCTTTTC CCATCTTTTC TCCAAAGGAA TAGAAATATC AATGTTCTAA AGTCCAGAGT 660 CACAGGATGA GGGTGTTGGG GGTAGAGCTC CTCCAGGGCC TGCACAAAGG TCCCAGGTCT 720 CTGCCTCTGA GCATGTGGTG GGGACCTGAG TCACCTTGCA AATGCACCCC AGCTTGGAGA 780 GCCTGCCCCG GCAGCTGCCC GACCCCTCCC AGGCCCAGCT GCTCCTCTAG GTCACTCAGG 840 AAGAAGCCTT GGGAACATCC TGGCCTGCCT GTGGCAGCAC CCTGGCAGGG TACCAGCTTG 900 GGGCCCTTCC TACCCTTGCG GGGAGCCAGC ATTGGAACCA CCCCGCTGAG TCTGGAAATC 960 CTCAGTTTTC TGACGCAGTT CCTCCTCAGC CACGAACGCA GGCAGAGCCT CCCCGGGGGG 1020 GGGCCCTGCA GCTCACCAGC TGCCGGTCTC TCCCCCAACC TCCCACGTCT CTTCCCACAC 1080 CTGCCTTCCA GTATTCTCCA GCACTTTGTC AGGATGCCTT AATGAGGCTA GGTTGCAGCA 1140 GGCCAGCAGC ATACTCACCT GGCTCAGGGA GTGTGACACA GCGTACGTGC TACCAAGAGC 1200 AGCTCCACTG AACTCCCATG TTGACAGCAG GGCCCTGCCT TCCCCGAACA TGGGCTGGCA 1260 AGTTTCCTCC ATCTCTCACC TTCTAAATCT ACTAGGAAGC CCTGTGGTAA AGCTCTCAGT 1320 CTCAGGCTGA GATTGCTGGG TTCAAATCCT ACCTCTCCTA CCTCTCCTAC TTACTAGGTG 1380 GAGTGACCTA ACCTCTCTGG GCCTTAGTGT TCTCATCTGT GAAAGGGGGA TAATAACCAT 1440 CCTGTATCAC AGGCTATTGT TGAGAATTAA ATGAGGCAAC ACATTGAAAG AGCTTAGAAA 1500 AATGCCTGGT ACATAGTAAG TGCTTATTAG ATGTCAGCTG TCATCTAGAT TTGCCAGGTG 1560 TCCTCTATGG TCATCAACAT TTAGTCCCTG CAGTGGGCAG 1600
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