| Tag | Content |
|---|
EnhancerAtlas ID | HS087-00705 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:36600680-36602160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr1:36601826-36601836 | TTCAAGTGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_01115 | chr1:36600144-36601228 | Adrenal_Gland | | SE_01115 | chr1:36601245-36603262 | Adrenal_Gland | | SE_01636 | chr1:36599006-36604267 | Aorta | | SE_02424 | chr1:36600639-36603153 | Astrocytes | | SE_04066 | chr1:36599670-36600906 | Brain_Anterior_Caudate | | SE_05887 | chr1:36598900-36604286 | Brain_Hippocampus_Middle | | SE_07920 | chr1:36599445-36602021 | Brain_Inferior_Temporal_Lobe | | SE_09456 | chr1:36600295-36601519 | CD14 | | SE_18752 | chr1:36600310-36602920 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_25992 | chr1:36600333-36603920 | Duodenum_Smooth_Muscle | | SE_26652 | chr1:36599084-36603413 | Esophagus | | SE_29723 | chr1:36600238-36601746 | Fetal_Muscle | | SE_31707 | chr1:36600547-36601256 | Gastric | | SE_31707 | chr1:36601697-36602607 | Gastric | | SE_35879 | chr1:36599757-36603157 | HMEC | | SE_37181 | chr1:36599594-36603933 | HSMMtube | | SE_38303 | chr1:36600107-36603567 | HUVEC | | SE_40420 | chr1:36600308-36601944 | K562 | | SE_42156 | chr1:36599361-36603351 | Lung | | SE_44877 | chr1:36600155-36603647 | NHLF | | SE_45971 | chr1:36598637-36604352 | Osteoblasts | | SE_48111 | chr1:36601275-36603098 | Psoas_Muscle | | SE_48599 | chr1:36599209-36603737 | Right_Atrium | | SE_51235 | chr1:36600791-36603416 | Skeletal_Muscle | | SE_53482 | chr1:36600002-36602420 | Spleen | | SE_54589 | chr1:36598907-36603542 | Stomach_Smooth_Muscle | | SE_56203 | chr1:36599115-36603890 | u87 | | SE_64044 | chr1:36601710-36603712 | HSMM | | SE_64339 | chr1:36598887-36603253 | NHEK | | SE_65351 | chr1:36598932-36601064 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 36601326 | 36601380 | | chr1 | 36602005 | 36602153 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I036133 | chr1 | 36598942 | 36603774 |
|
Enhancer Sequence | CTTGTTGGGA GGGAATGGCC TAGCTTAGGG GGCTGTCTCA GCCTCACAGT CATAGTAAGA 60
GAGGAATGTG TAATCTACAA CCAATCAATG ACATGGGTGG GGACCAGGAA GTTAGTTTCC 120
TGGGGATTGC ATGTTCCAAA TACTTCTGCA GTCCCCAGCT CTTTCTTTCC CTCAGCCCCA 180
ATCGTGGGGC TGTAACTGGG AAAAGTCACT AAGGGAGCTT TGTTTCCACA GTTCCCTAAT 240
CCTGTAATGT TGCCCAAGTT TAACATTGGG AAAGGAAATA TCCAAAACGT CACGACATAC 300
AAACCGCTGC TCAAAAGTAG GCTGTGGTAC CCGGAGGAGA GGAAGGGCCG AGGGTCCCCC 360
TGGAGAAGGG AAAGGGCGGT GTAGCTTTTT TTGGCAGGGT TCAGACACTA CATAAAGCTT 420
TCCACATCTG GGCCCCAACA TTCATTCCCT TATTCATTCA TTCAGACTCT GGTGTGACTG 480
GACTGAGACC CACACTAAGT GCTAAGGACA CAGTTAACCA AAATTGAATC ACTGCCCTGG 540
GACCCCAAAT TATAATATGG AGGGGGACAT AAAGAGGCTC AGAGGATGTT CCTATATTTG 600
GGGACACGAA ACTGACCATC CCTCTTTGGT GGCCTAATCC AGCTAGAGCC GGTAAGTCCT 660
TGCAAACTGC CCTTCTCAGT GGTGTCTCAA AACCCTGGTC CTACCCTTGC ACAACCAAAA 720
CACATCTCAA GCACAATGCA TCTAAAACTG GCTCCCCCCA TCTCAGGCCT GCACACATAC 780
TTTAGGGAAG GCCTGGGACC CCATTTCCCT CCAACAACCT GAGTGTCTAG ACCTCAGGGC 840
CTTAGGCTAT CCCCAAGCAG TGCTACCAAA TACAGCCTGA CACAATCTCT GCTTCCTCCT 900
TTTAAGATCT ATCCCAAGCT CTCTAAGCCT GGGAGAGGGA GCTGTGGCCT GTTCCCTTTT 960
TCCCCCATAG TGTTAACCAG GCAGTAAAAG AATCTTCATT AAGAGCATGG GTTTTGCCCT 1020
TTGGCCCAGC TTTGAACCCT AACTTTTCCA CTTACTCACC ATATGACCTG GGCAACTTAT 1080
GGCCTCCACT CTAAAAATGG AATTCTTGTG AGCTGGCCAA TGCATGCAAA GTGTTCAGTA 1140
GTGTCTTTCA AGTGGTAAGC ACTCAACAAA TAGCACCCCA ACAACAGGGT TTATATGGCC 1200
TTTCTAGCCA GACCTTCCAA CTTGGTGGCC AAGTGCCCAG GATAGTTCAT TTTAGGTATG 1260
TCTGGAATAA TGGTCTGCTT CTAGATTTTG CTGCACACAC TAGAGCCAAA AGCGACTCTG 1320
AAGGGGCTTC AGTTGCTTAT ACTGGCTCCC AGGTTTCCCA GACACTCTCG TCTGTGGAGA 1380
GAAGCCACTG CTAAACCAAG TCAAAGAAAG ACAGGGCCCA TGAACCTACC TGGTCTCCTC 1440
ACACCATTGT AACAAAACAC CTGGGGATAA GCAGAAAGAA 1480
|
