| Tag | Content |
|---|
EnhancerAtlas ID | HS020-31950 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr3:129343140-129344910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr3:129344090-129344105 | GGATGTGGGTGGTCC | - | 6.19 | | Zfx | MA0146.2 | chr3:129344740-129344754 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00112 | chr3:129340805-129347842 | Adipose_Nuclei | | SE_00978 | chr3:129340996-129344782 | Adrenal_Gland | | SE_01893 | chr3:129341768-129344979 | Aorta | | SE_04322 | chr3:129343992-129347508 | Brain_Anterior_Caudate | | SE_05345 | chr3:129343446-129347451 | Brain_Cingulate_Gyrus | | SE_05951 | chr3:129340827-129347709 | Brain_Hippocampus_Middle | | SE_07365 | chr3:129343956-129347550 | Brain_Hippocampus_Middle_150 | | SE_09767 | chr3:129342751-129347601 | CD14 | | SE_26494 | chr3:129343406-129347432 | Duodenum_Smooth_Muscle | | SE_27065 | chr3:129341010-129343494 | Esophagus | | SE_27065 | chr3:129343609-129344791 | Esophagus | | SE_29874 | chr3:129343657-129347429 | Fetal_Muscle | | SE_31569 | chr3:129341039-129347353 | Gastric | | SE_37506 | chr3:129343906-129347484 | HSMMtube | | SE_37994 | chr3:129339897-129347523 | HUVEC | | SE_40701 | chr3:129340197-129347529 | Left_Ventricle | | SE_42115 | chr3:129332899-129347478 | Lung | | SE_46476 | chr3:129343823-129347545 | Osteoblasts | | SE_47266 | chr3:129343410-129347403 | Panc1 | | SE_48609 | chr3:129340064-129347458 | Right_Atrium | | SE_50249 | chr3:129340253-129347425 | Sigmoid_Colon | | SE_51354 | chr3:129340749-129347601 | Skeletal_Muscle | | SE_52687 | chr3:129340963-129344810 | Small_Intestine | | SE_53375 | chr3:129340176-129347496 | Spleen | | SE_62855 | chr3:129293187-129347490 | Tonsil | | SE_65523 | chr3:129341199-129347466 | Pancreatic_islets | | SE_68869 | chr3:129343741-129347394 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I129621 | chr3 | 129340226 | 129347832 |
|
Enhancer Sequence | TACAAAAAGT TAGCTGGGCA TGGAGGCTGC TGCCCGTAGT CTCAGCTACT TAGAGGACCG 60
AGGTGGGAAG ATGGCTTGAG CCCAGGAGGT CAAGGCTGCA GTGAGCTGTG GCTGTACCAC 120
TTGCACCCTC CAGAACTGAG AGGAAATAGG TTTCTGTTGT TGAGCGATCC AGTCTGTGGC 180
CTCTTGTTAC GGCAGCCTAG CAAGCAAACC TCCCCCTGGC CCCGTGACCT CTCCCGCTGT 240
TCTGGAGGCT GCAAGGCCAA GTCCAAGACC AAGGAGTCTG CAGGGTTGGT GTCTGCTGCA 300
GCCTCTCTCC TTGGCTTGCA GATGGTGCCT TCTGGCTGTG TCCTCACATG ATCTTCCCTC 360
ACTTCCTGCA TATCTGAATC CTCAGCTCCA CTTCTTTATT TTTTTTTTTT TGAGACAGGG 420
TCTGACTCTG TCACCCAGGC TGGAGTGCAG TGTTGCGATC TCAGCTCACT GCAGCCTCGA 480
CTTCCTAGGC TCAAGCCATC CTCCAACCTC AGCCTCCTGA GTAGCTGGGA CCCCTGGCAG 540
AGGCACCATC GAGGCTTCCC TTTGGCTCTC CGCTCCAGCA GCACTGGCCT CCTCACTGAG 600
CTTGGTCCAG GACGGTGCTT TTGCTGTGCC TTCTGCCTGT CATGCCCTTT CCAGATCTCC 660
CCAGGGCTGC CGCCTTCTTA TCCCTCAGGT TTCTGCTCAA ATATCCCCCT CCAAAGAGGC 720
CCTCCCTGAC CAAAGTGCCA ATCAGGGCTA GTATCCATCT CTCTCACTGG ATGGACCTTC 780
ACCAGGGCAG GGGATATGTC TCCAGGGCCA CAGCAGGGCC CGGCACACAG TAGGTGCACA 840
GTAAAGGTTT GCTGAAGGCA GTCAGGCTCA CCTTGGTACT GCCACCCCAT CTCCCAAAAC 900
ACAGGGTCAC AGGGTCTCAG AGGCAGAGCA GGGCCTCCAG GGGGGCCCGT GGATGTGGGT 960
GGTCCAACCA TGAGGACTGC CTACCTGCTG GGGGCACAGG CTGCAGCCAC CCATCCCCTC 1020
GGCTTCCCAC GCAGCACCTG TGTTCACCGC CCCCTTCCCC ATCTGTCTTC CAGTGATTCC 1080
TCCAGAGGCT GCTTGTTTGG GAAGAAGGCT AGATGGCTAA GCAGGTAGGA CCAGGTGGAA 1140
ACACAGCCCA TCACTTTGGA CTTGGGGACT CTGCCAGTGC CTCCCTGCTC CAGTGTCTGA 1200
GGAGGACTTG AGCATAGGAA GGTGCGTGCC TGCTCAGTCC TGGGACTCGT GGGGTGGAGC 1260
ATTCACCTGG GGACTCGTGG GGTAGAGCTG GGGCTGGGAC CACTGCCTGC ACCTCCATCT 1320
GGGAGCAGGA TGAGGGAAGG GCAGGAAACC ACTGGGAGGC GCTGGGTGGG AGTTCGCTCT 1380
TTGCTCAGTC AACCCTGTCT TGAGACAGCC CTACTCCCAC TTGAAAGGCT GAGACAGAAA 1440
AGACTGACAC CACCAAGTGT GGGTGAGGAT GTGGAGCCAC AGGGGCAGGG GTGAAATGTG 1500
AAATGGTGCA GCCACTCTGT AAAACCTTTT GCTAGTTTCT TCAAAAAAAG TCAAATGTGG 1560
CTGGACGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG CGGGCGGATC 1620
ACGAGGTCAG GAGATAGAGA CCAGCCTGGC TAACACGGTG AAACCCTGTG TCTACTAAAA 1680
ATACAAAAAA AATTAGCCGG GCGCGGTGGC AGGCGCCTGT AATCCCAGCT ACTCAGGAGG 1740
CTGAGGCAGG AGAATGGCAT GAACCCGGGA 1770
|
