Tag | Content |
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EnhancerAtlas ID | HS180-44697 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:44670250-44671490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:44671431-44671449 | CCTTCCCTCTTTCCTTTC | - | 6.62 | ZNF263 | MA0528.1 | chr7:44671419-44671440 | CCCTCTCCACCCCCTTCCCTC | - | 6.04 | ZNF263 | MA0528.1 | chr7:44671401-44671422 | TTTTCTCTCTCTCTCTCCCCC | - | 6.12 | ZNF263 | MA0528.1 | chr7:44671409-44671430 | CTCTCTCTCCCCCTCTCCACC | - | 6.1 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_09293 | chr7:44668114-44680616 | CD14 | SE_12002 | chr7:44669441-44675480 | CD3 | SE_14587 | chr7:44668357-44680825 | CD4_Memory_Primary_7pool | SE_15490 | chr7:44669686-44672394 | CD4_Memory_Primary_8pool | SE_16434 | chr7:44669479-44672486 | CD4_Naive_Primary_8pool | SE_16951 | chr7:44669426-44675446 | CD4p_CD225int_CD127p_Tmem | SE_17851 | chr7:44668129-44680829 | CD4p_CD25-_CD45ROp_Memory | SE_18656 | chr7:44670100-44680815 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19294 | chr7:44669461-44675423 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20655 | chr7:44668188-44680617 | CD56 | SE_21218 | chr7:44669359-44672271 | CD8_Memory_7pool | SE_22840 | chr7:44669573-44672271 | CD8_primiary | SE_26120 | chr7:44669675-44671706 | Duodenum_Smooth_Muscle | SE_27427 | chr7:44671324-44672207 | Esophagus | SE_27654 | chr7:44668239-44680825 | Fetal_Intestine | SE_28557 | chr7:44668586-44680821 | Fetal_Intestine_Large | SE_32407 | chr7:44670260-44670796 | Gastric | SE_32407 | chr7:44671362-44672401 | Gastric | SE_34691 | chr7:44670606-44681894 | HeLa | SE_37328 | chr7:44666429-44672269 | HSMMtube | SE_40682 | chr7:44670989-44672225 | Left_Ventricle | SE_42544 | chr7:44669345-44672207 | Lung | SE_43768 | chr7:44668130-44675212 | MM1S | SE_50531 | chr7:44668334-44672228 | Sigmoid_Colon | SE_52560 | chr7:44669281-44671462 | Small_Intestine | SE_53907 | chr7:44668196-44672382 | Spleen | SE_62947 | chr7:44653723-44680812 | 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 |
GH07I044628 | chr7 | 44668008 | 44681598 |
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Enhancer Sequence | TATAAACTAT GCACGTTCTC CCATATACTT TAAATCATCT CTAGATTACT TGTAATACCT 60 AATACAAGGT AAATGCTATG CAGATAGTTG TTATACTTCA TTGTTTGTGG CAGCAGTCCC 120 CAACTCCTTT GGCACCAGGG ACCAGTTTCG TGGAAGACAA TTTTTCCATG GACTGAGGGA 180 TCAGGGGAGG ATGGCTTTGC AGTGAAACTG TTCCACCTCA CATCAGGCAT TAGTTAGATT 240 CTCATAAGGA GTGAACTTAG ATCCCTTGCA TGCACAGCTC ACAATCCAGT TGGCTCTCCC 300 ATGAGAATCT AATGCCCCCG CTGATGTGAC AGGAGGTGGA GCTCAGGTGG TAATGCTCGC 360 TTGCCGCTCA CTTCCTGCTA TGCAACCCAG TTCCAAACAG GCCACTGACC AGTACTGGTC 420 TGTGGCCCGG GGGTTGGGGA TCCCTGGTTT AGAGAATAAT AACAGGAAAA AAAAGTGTAC 480 ATGTTCAGTA CAGGCAGTTT TTTACCAACT ATTTTCAATC CACGTTTGGT TGAATCCATG 540 GATGCAGAAC CCACAGATAC GGAGGGCTGA CTGTATACAT AAACTGCATG GTCTACGTAA 600 ATGGGGTTTC AGCGATGAGC TTTGAAGTTA CCCCTTGATG ATTTTTTGTT TTTGAAGATT 660 CAGGAGGTAC ATGTGTGGGT TTGTAACATG GGTACGTTAA GTAATGGTGG GAATTGGGTT 720 TCTAGTGTAC CCATCACCCA GATAATGAAC ATTGTACCCA ATAGGCAATT TTTCAACCCT 780 CACTCTCCTA CCACCCTCCC CCACCGCCAC TTGATAATCT TTAACTTCAC ATGTTAAGAG 840 CAATCTCAGC ACTTGTGGCT TTTTGTGTTA AATCAGCTAA ACTGACTGAG TGCGCCTTCT 900 CCAACTTTAG CACAGTATTT CACTCTTAAG CAGTTTGCAT TTATGGTTTA TTTAGGGTGA 960 TAAAATTATA ACCTCTTTGA AACAACAGGA AACATGAAGC AACACCCTCA CTTGTGTGGT 1020 AGTTTGCAGC TCATGACAGC TGTGTTCGAA GCTTGTGCTG AGTGGCGGCT GCAAGAGGAA 1080 AAGCAGTCTT GCCCTGTTAT CCTAGCAGGA TGATTAAATA AGTTTAAACA ACAGTTAAAA 1140 TTCTAGCTCT CTTTTCTCTC TCTCTCTCCC CCTCTCCACC CCCTTCCCTC TTTCCTTTCT 1200 CTCTCCTCTC TCTCCCGGCC CTTAAAAAGA AAAATAAATA 1240
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