| Tag | Content |
|---|
EnhancerAtlas ID | HS051-27827 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr9:130861050-130863370 |
Target genes | | Number: 43 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr9:130861276-130861291 | GTGTTCCTGAGAAGT | + | 6.34 | | Tcf12 | MA0521.1 | chr9:130862583-130862594 | AACAGCTGCTG | + | 6.32 |
|
| | Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
| SE_00502 | chr9:130859402-130866004 | Adipose_Nuclei | | SE_01177 | chr9:130859439-130863274 | Adrenal_Gland | | SE_02078 | chr9:130859356-130863981 | Aorta | | SE_02461 | chr9:130859304-130863114 | Astrocytes | | SE_08626 | chr9:130858493-130862947 | Brain_Inferior_Temporal_Lobe | | SE_09846 | chr9:130858639-130861849 | CD14 | | SE_13739 | chr9:130859872-130862337 | CD34_Primary_RO01536 | | SE_23076 | chr9:130858917-130863198 | Colon_Crypt_1 | | SE_23771 | chr9:130859824-130862455 | Colon_Crypt_2 | | SE_24841 | chr9:130859798-130862587 | Colon_Crypt_3 | | SE_24841 | chr9:130862748-130863210 | Colon_Crypt_3 | | SE_25948 | chr9:130853911-130863239 | Duodenum_Smooth_Muscle | | SE_26752 | chr9:130858869-130863439 | Esophagus | | SE_27710 | chr9:130859695-130863223 | Fetal_Intestine | | SE_28658 | chr9:130859472-130863226 | Fetal_Intestine_Large | | SE_29715 | chr9:130859418-130863519 | Fetal_Muscle | | SE_31462 | chr9:130859415-130863392 | Gastric | | SE_37200 | chr9:130859386-130867552 | HSMMtube | | SE_41771 | chr9:130860702-130862161 | LNCaP | | SE_42378 | chr9:130858694-130866135 | Lung | | SE_44311 | chr9:130858792-130863921 | NHDF-Ad | | SE_44961 | chr9:130859352-130863261 | NHLF | | SE_46195 | chr9:130858607-130863783 | Osteoblasts | | SE_46747 | chr9:130859844-130863392 | Ovary | | SE_47545 | chr9:130859779-130867121 | Pancreas | | SE_48196 | chr9:130859594-130867368 | Psoas_Muscle | | SE_49302 | chr9:130858827-130865482 | Right_Atrium | | SE_51250 | chr9:130858612-130867152 | Skeletal_Muscle | | SE_52155 | chr9:130859855-130862521 | Skeletal_Muscle_Myoblast | | SE_53470 | chr9:130859373-130864872 | Spleen | | SE_55063 | chr9:130858770-130863497 | Stomach_Smooth_Muscle | | SE_63942 | chr9:130859841-130862657 | HSMM | | SE_65681 | chr9:130859040-130867370 | Pancreatic_islets | | SE_66839 | chr9:130859883-130862106 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTGTTGAGT GAATGGCTGA GCATGCATGA ACCATCCCCC ACTGAGAGGA AAGAATGTCT 60
GAAATGTAGC AGTTTTTTCC CATTGCCATG CGGCTATGGC CGGCACGTGT ACGTCACAGG 120
AGTGACCGGT TTTCATGTGA CTTCCCAGGA AGGCTGGAAT TCCAGCGAAG GCTGTTGTGA 180
GAAATGGACT TTCAGAAAGG AAATTCCTTT TGCTGGAATG AGGGGGGTGT TCCTGAGAAG 240
TACAGAGCCA GAAAGGGACC TGGGGGGCAG GCCAGTAGTG CATGGGAGGA GAAGGCAGGG 300
AGGCCCAGGA GTTGAGGGTG CTGCGTGGTG GAGCTGCCCG TCCCTGGTGT GGGGGTGAGG 360
GAGCCTCCCG CCTTCTCGAC TCTCAGACAT CGCTGTGGAA CAGGGCCTGT GTCTGCCCTG 420
AAAGTGAGGA AGCCGAGCTG CAGAGTCCGG AGGCCCCTTG CCACCTCGGC TTCTCGGTTA 480
ATCAGTTTCC CTGCTACCCC CAGTGCCCAC TGTGCACCAA GGGGGATTTG CAGATCCAAG 540
GAAGGAGACA GAAGGAGGCC CAGGCCCTGT GAGGCAGAAG CAAGCACTTT GAGAATGCGT 600
TGAAGCCAGC TGCGGTGAGC ACACCCTCTG CTCTGGGTGT CTGCGACAGC ACCCACCCCA 660
GGGAGGCATG TGGCTCACCC TGGCAGCAGG CGGCTGGGTC CCAGAGGGCT CCATGCCTGA 720
TGTTCGCCTC CTGCCTAAAT GGCTTGTCCA CTCTATTTCC ATTCCTGTTA GAGATTTGGA 780
GCAGTCACCC TATAGGTGAT TTATGTCACT CTTGTCTGAG AGCACAGATG TCCACAGGAA 840
GTTAAATGTA ACCTCAGCAG ATAAAATATG TACCTGCATC TGTCCTACAT TCCAGCCACG 900
CCCCTCACAT TAGCCTTTTG ATCGCGCCAG GTCATGGGGT ATCTGTTCAG GCCTCCCTGC 960
CCCTGACACC TTTGGCAGCT GAGGAATCAC AAGGCGCTGT CAGTAGTGTG TCTAAGAGAG 1020
AGGCGCGGTG GTGATCCTTT GAGGACGCGA GCTAGCCAGT GGGCCATCCA TTTCCAAACC 1080
CCAGCTGGCT GTCAGTTGAT TTCTCCCAGT GAGAAATCCG GAGGACACAG GAAGACTATA 1140
CCATCTTCCT TGGGAGATTC TCGGTCCCAG TTTTGGGTTC CGGATTCAGG GCGTTGCTGA 1200
GTTGGGGTGA CTCACTTTCA TCCCCCATGT TCTGAAGGTT AGCCTTGAGG GTGGCGGCAG 1260
GATGTGCAGG GAGGCGGCTT GGGAGGACCA CGGCCCAACT TGCATCCCGC CCACCACTTC 1320
CCTAGCTGTC TGACCTTGTG TAAATGTTTA GGCTCTCGGA ACTCCTGTTT CCTTCTCTGT 1380
AAAATGGGGG AAATGACATT TCCTACCTCC TAGAGCTGTT TGCGAGGGGG GTAAGTGGGT 1440
TGCTAGAAGT AAAGCATTTG GCACGCCCTG CGGCCGGTGC TAGGTGCTGG GGAAATGTGT 1500
GCTCTCGTGG AGCTGTCCCA GTTGCCAACC ATTAACAGCT GCTGAACAAA GCCCACCTCC 1560
TGGGAGGCGG GGGCGGGGGG GGTTACTTTT GGAACCTCAT TGCCAAGGAA CAGTCTCTCA 1620
AAGCCTTCTT GGGACACTAA AGTGCTTTTC AGTGAGTGAG CGGGAGAGCC AGGGCAGCTC 1680
TATCACCTGG CTTCCCTGAG AGCAGGGACT GGCAGTACCA TCATACACAT GCCCTTGGCT 1740
CCTTACACTT CCCCGGCCTC GGGTGCTGTG GCAGAGTCTG GCTCTGCCCC CGATTTTCAC 1800
CTGCCCACCA AATTATTCTC GGACCAATGC CAGTTTTAGG AGAGAAACAG CGAGCTGCAG 1860
AGTTCCTGTC AGAAACTGGA CTCCATGGCC ATCCCCAAGT CTCAGCAGGG AGCATGTGTG 1920
GTTGAAGCCT GGGTCCAGGG ACCCAGGGAC GGCGCTGCAG CGAAGCCACC CTGCTCACCC 1980
TGGCTGTACG GCACGCAGGT CTTCAGACTG AGAAAGTGCC CAGCTGTCCC TGTCGGCCTC 2040
TGTCCGGAGG GCTCTTCCCA GGCTCCTTGT TTCCTCTCTG CTTGAGAGGG AGACAAGATT 2100
GGCCCTTGCC TGGGTTCTGG CCAGCACCTG GGGTTCTAGG TGGTGGCTCT GGCATGTAAG 2160
TCGATTGCCA TGGTGGCTCT GAGAGTGGAG CAGAAGCATC TTGGGTCCTT GGGGCCAGCT 2220
CTGCTCGCAA TTAGTGAAGT CATTGCCTGG GGATGGGGCC CCACAAGGGA CAAGGAAAGG 2280
CTGGTCCAGG AGCCAAAAGA CAAAATGTTA CCTTTCTTTT 2320
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