Tag | Content |
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EnhancerAtlas ID | HS105-80719 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:33150850-33152290 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I033149 | chr9 | 33149003 | 33152397 |
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Enhancer Sequence | CCTGGGAAAT AGAAGTGGGA ATGAGGACAA AATAAAACAA ATACATGAGG CAAGAGAGTC 60 CATGAGTAGA CCCCAATGAT GATTATTGGC CATGAAAGGA AGCTTGATGG CTGGATGGAA 120 AGAAGGAAGG AAGGAAGGAA ATAAGTAAGG GAGAGATGGC GGATGGAGCT GGATGTGTCC 180 TTCCAGGGCT GTACAAAGGA GGGGGACCCC AACCCCTAGT CCAGACAAAG GTCCCTAAGG 240 CAGGTGTACA GTATTGTGGG GATGAATTCA TCAGCCACGA GAGACTGACC CATCTAATGT 300 TAAATTCACT TCCCTGCTCT GACTGCTGAC TCACCAGCAG TTAGCTTATC CTGCGGCTTC 360 CCTTGCAGTG AATTCAGCCA GAGATTTCTA AGCTACTCAA TAACAGTTCT AATCTTCCCA 420 GTAAAGCTGC AACTTTGCAT TCCAGTATGT AAGTAAGTCT CCTGGGAGTT TTATTACTGA 480 GTCAGCTGCC CCTCTAATCA GTTTTGGAGC CCCAGCAGAT TTTCTGGAGC TGCGGTGCTG 540 ACTACGAGCA CATCCTTCTC TCTCCACCTA GAACCAGACC TTGGACTGTG GAGGGCCCAC 600 TACTCCTATG GGCCATCTGG GCACTCAGCC AGCCAAGTAC TCCTGGCAAT ATCTCTCTGG 660 TGTCAGGACT ACTTTAAATG TAGCCAGCTC CAATTTCCTT CTCTAAGGAG TGGGGATAAT 720 TATGCCTTCC TTTCAGATGT AAGTGAAATA ATACATATAC ATACTTATCG CATGTTCTTA 780 TTGAGCTAAT AGATGTTCAA TAAATGTTAC TTTCCCTTCT CCCCTGACTC CTTAGAACTT 840 CAGAGCTTAC AAATTACTAC AGCTCTATCA GCACACATGG CTAAATTTTC ACATTTCTAC 900 TCTTAGCCAC TAGAATCACT GATAGATTTG GAGGAAAACT CTGGGACCTT AAAGGGTCCC 960 TGGAGTATTA CATAAAGCTT CTTGCAGCAT GAGAGTTGAA CAGAAATTCT GTTCATCTTT 1020 TGCTGTCGAA GCCAAGTTGG TGGCTTCTAA AGAACCAACT TAGAAGAAAA CTCAGGAGAA 1080 AAATTTTATC ATTTTGGGAT GGTGAAGACC TGCTTAAGTA TGAAAGCAAC CTGAAGTCAT 1140 AAAGGAAAAC ATAGATTTAA ACACATAAAA ATTCAAAACT TCTGGCCGAG TGCAGTGGCT 1200 CACGCCTGTA ACCCCAGCAC TTTGGGAGGA TCATTTGAGA TCAGGAGTTT GAGATCAGCT 1260 TGACCTACAT AGTGAAACCC CGTCTCTACT AAAACACAAA AATTAGCTGG GTGTGGTGGC 1320 GGGTGCCTGT AATCACAGCT TCTCGGGAAG CTGAGGCAGG AGAATCGCTT GAACCCAGGA 1380 GGCAGAGGTT GCAGTGAGCC GAGATTTCAC CACTGCACTC CAGCCTGGGC GACAGAGCAA 1440
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