Tag | Content |
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EnhancerAtlas ID | HS108-40504 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:33150780-33152100 |
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) |
EWSR1-FLI1 | MA0149.1 | chr9:33150982-33151000 | GGAAGGAAATAAGTAAGG | + | 6.5 | EWSR1-FLI1 | MA0149.1 | chr9:33150978-33150996 | GGAAGGAAGGAAATAAGT | + | 6.7 | EWSR1-FLI1 | MA0149.1 | chr9:33150962-33150980 | GGATGGAAAGAAGGAAGG | + | 7.73 | EWSR1-FLI1 | MA0149.1 | chr9:33150974-33150992 | GGAAGGAAGGAAGGAAAT | + | 9.03 | EWSR1-FLI1 | MA0149.1 | chr9:33150970-33150988 | AGAAGGAAGGAAGGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr9:33150966-33150984 | GGAAAGAAGGAAGGAAGG | + | 9.47 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00330 | chr9:33150154-33152533 | Adipose_Nuclei | SE_00992 | chr9:33150845-33151621 | Adrenal_Gland | SE_03080 | chr9:33150830-33151209 | Bladder | SE_09459 | chr9:33150683-33152077 | CD14 | SE_10229 | chr9:33150691-33152191 | CD19_Primary | SE_10912 | chr9:33119344-33169982 | CD20 | SE_19329 | chr9:33150695-33152114 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20045 | chr9:33150690-33152312 | CD56 | SE_22416 | chr9:33150710-33152253 | CD8_primiary | SE_23687 | chr9:33150875-33151683 | Colon_Crypt_1 | SE_26031 | chr9:33150287-33152385 | Duodenum_Smooth_Muscle | SE_26859 | chr9:33150779-33151670 | Esophagus | SE_27770 | chr9:33149455-33152321 | Fetal_Intestine | SE_28724 | chr9:33149325-33152320 | Fetal_Intestine_Large | SE_29800 | chr9:33150488-33152194 | Fetal_Muscle | SE_31534 | chr9:33150777-33151683 | Gastric | SE_34775 | chr9:33150487-33152230 | HeLa | SE_40894 | chr9:33150769-33152080 | Left_Ventricle | SE_41831 | chr9:33150862-33151334 | LNCaP | SE_42236 | chr9:33150804-33151823 | Lung | SE_44340 | chr9:33150635-33152125 | NHDF-Ad | SE_45447 | chr9:33150452-33151912 | NHLF | SE_45731 | chr9:33149399-33152178 | Osteoblasts | SE_46917 | chr9:33150883-33151589 | Ovary | SE_47814 | chr9:33151298-33151559 | Pancreas | SE_48426 | chr9:33150761-33152145 | Psoas_Muscle | SE_48738 | chr9:33150773-33151797 | Right_Atrium | SE_50176 | chr9:33150800-33151701 | Sigmoid_Colon | SE_51651 | chr9:33149245-33152315 | Skeletal_Muscle | SE_52621 | chr9:33150782-33151822 | Small_Intestine | SE_53402 | chr9:33150804-33151863 | Spleen | SE_56627 | chr9:33150139-33152742 | u87 | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 33150936 | 33151964 | chr9 | 33150828 | 33152043 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I033149 | chr9 | 33149003 | 33152397 |
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Enhancer Sequence | CTTCCATTTT GGCAAGAGCA AAAACAGATA CACAAACTAT AAATACGTTA GAATAGTTGC 60 CTGTGATATA CCTGGGAAAT AGAAGTGGGA ATGAGGACAA AATAAAACAA ATACATGAGG 120 CAAGAGAGTC CATGAGTAGA CCCCAATGAT GATTATTGGC CATGAAAGGA AGCTTGATGG 180 CTGGATGGAA AGAAGGAAGG AAGGAAGGAA ATAAGTAAGG GAGAGATGGC GGATGGAGCT 240 GGATGTGTCC TTCCAGGGCT GTACAAAGGA GGGGGACCCC AACCCCTAGT CCAGACAAAG 300 GTCCCTAAGG CAGGTGTACA GTATTGTGGG GATGAATTCA TCAGCCACGA GAGACTGACC 360 CATCTAATGT TAAATTCACT TCCCTGCTCT GACTGCTGAC TCACCAGCAG TTAGCTTATC 420 CTGCGGCTTC CCTTGCAGTG AATTCAGCCA GAGATTTCTA AGCTACTCAA TAACAGTTCT 480 AATCTTCCCA GTAAAGCTGC AACTTTGCAT TCCAGTATGT AAGTAAGTCT CCTGGGAGTT 540 TTATTACTGA GTCAGCTGCC CCTCTAATCA GTTTTGGAGC CCCAGCAGAT TTTCTGGAGC 600 TGCGGTGCTG ACTACGAGCA CATCCTTCTC TCTCCACCTA GAACCAGACC TTGGACTGTG 660 GAGGGCCCAC TACTCCTATG GGCCATCTGG GCACTCAGCC AGCCAAGTAC TCCTGGCAAT 720 ATCTCTCTGG TGTCAGGACT ACTTTAAATG TAGCCAGCTC CAATTTCCTT CTCTAAGGAG 780 TGGGGATAAT TATGCCTTCC TTTCAGATGT AAGTGAAATA ATACATATAC ATACTTATCG 840 CATGTTCTTA TTGAGCTAAT AGATGTTCAA TAAATGTTAC TTTCCCTTCT CCCCTGACTC 900 CTTAGAACTT CAGAGCTTAC AAATTACTAC AGCTCTATCA GCACACATGG CTAAATTTTC 960 ACATTTCTAC TCTTAGCCAC TAGAATCACT GATAGATTTG GAGGAAAACT CTGGGACCTT 1020 AAAGGGTCCC TGGAGTATTA CATAAAGCTT CTTGCAGCAT GAGAGTTGAA CAGAAATTCT 1080 GTTCATCTTT TGCTGTCGAA GCCAAGTTGG TGGCTTCTAA AGAACCAACT TAGAAGAAAA 1140 CTCAGGAGAA AAATTTTATC ATTTTGGGAT GGTGAAGACC TGCTTAAGTA TGAAAGCAAC 1200 CTGAAGTCAT AAAGGAAAAC ATAGATTTAA ACACATAAAA ATTCAAAACT TCTGGCCGAG 1260 TGCAGTGGCT CACGCCTGTA ACCCCAGCAC TTTGGGAGGA TCATTTGAGA TCAGGAGTTT 1320
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