| Tag | Content |
|---|
EnhancerAtlas ID | HS047-28358 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:7157070-7158960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr6:7158510-7158528 | GTTCAGGTTTAACTTTCC | - | 6.08 | | Lhx3 | MA0135.1 | chr6:7157358-7157371 | GACTAATTAATTA | - | 6.46 | | POU4F2 | MA0683.1 | chr6:7157356-7157372 | ATGACTAATTAATTAG | + | 6.31 | | mix-a | MA0621.1 | chr6:7157362-7157373 | AATTAATTAGT | + | 6.62 | | mix-a | MA0621.1 | chr6:7157359-7157370 | ACTAATTAATT | - | 6.62 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00099 | chr6:7150760-7175124 | Adipose_Nuclei | | SE_01064 | chr6:7156909-7157399 | Adrenal_Gland | | SE_09175 | chr6:7150259-7157560 | CD14 | | SE_09175 | chr6:7157614-7160672 | CD14 | | SE_11591 | chr6:7151171-7157857 | CD20 | | SE_13456 | chr6:7152346-7157404 | CD34_Primary_RO01536 | | SE_23267 | chr6:7158358-7158959 | Colon_Crypt_1 | | SE_24175 | chr6:7156917-7157366 | Colon_Crypt_2 | | SE_26179 | chr6:7155827-7157592 | Duodenum_Smooth_Muscle | | SE_26569 | chr6:7156004-7159037 | Esophagus | | SE_30159 | chr6:7153789-7157484 | Fetal_Muscle | | SE_31471 | chr6:7156479-7157355 | Gastric | | SE_31471 | chr6:7157812-7159002 | Gastric | | SE_32706 | chr6:7152529-7158442 | GM12878 | | SE_35642 | chr6:7157804-7163763 | HepG2 | | SE_37264 | chr6:7153761-7159594 | HSMMtube | | SE_41219 | chr6:7156041-7157496 | Left_Ventricle | | SE_42377 | chr6:7156013-7157585 | Lung | | SE_42377 | chr6:7157749-7158821 | Lung | | SE_43730 | chr6:7154650-7157540 | MM1S | | SE_45215 | chr6:7156500-7157614 | NHLF | | SE_46025 | chr6:7155667-7160190 | Osteoblasts | | SE_50177 | chr6:7156036-7157572 | Sigmoid_Colon | | SE_51588 | chr6:7153835-7157377 | Skeletal_Muscle | | SE_51921 | chr6:7153969-7159058 | Skeletal_Muscle_Myoblast | | SE_52972 | chr6:7155944-7157485 | Small_Intestine | | SE_53741 | chr6:7156781-7157462 | Spleen | | SE_54903 | chr6:7155996-7157477 | Stomach_Smooth_Muscle | | SE_59725 | chr6:7099938-7157593 | Ly4 | | SE_63714 | chr6:7153896-7159166 | HSMM |
|
| | 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 |
| GH06I007150 | chr6 | 7150768 | 7159561 |
|
Enhancer Sequence | CCTGAGTAGG AGGAGAGGGT TCCAGAGTGC CACTTGGCTG CTCCTGTGTA CCCATTCTTG 60
TTCAAGAGCA CCTTGAGATC ACATGGTCTT AAATGCCAAA GCTGACCAAG AGCTGCCCCT 120
CTGTTCAGCT TCGTCGTCCC TGGCTGTTGG GGAGGACTTT GTCTGTCTGA CTGCCGCTGG 180
GCTGCCTTGC CCCAGCTCCC TGGGGTCCTT TGCTCCGTAA TCCATCAGCT CTTCTTTTCT 240
CTTCTTCTTA CTCATAGTAT AAGACCCGAC TGCCCATTTT TTGGAGATGA CTAATTAATT 300
AGTAAAATAT TTGGCTGGGC GCGGTGGCTC ACGTCTGAAA TCCCAGCACT TTGGGATGCA 360
GAGGCAGGCA GATGGCTTGA GTTCAGGAAG TTGGAGACCA GCCTAGGCAA CATGGTGAAA 420
CCCTGTCTCT ACCAAAAATA CAAAAACTTA GCCAGGTGTG GTGGGGCGTG CCTGTAGTCC 480
CAGCCACTTA GGAGGCTGAG GCACAAGAAT TGCTTGAACC CGGGAGGTGG AGGTTGTAGT 540
GAGCCAAGAT CGTGCAGCTG CACTCCAGCC TGGGCAACAG AGTAAGACTC CATCTCAAAA 600
AAAAAAAAAA TTGAGTGCCT ACTGTGTGCA CATGTACCCT GTGTGACCAT GGGCCAGGCA 660
CAGTGGTTCA TGCCTGTAAT CCCAGCACTT TGAGAGGCTG AAGCAGGTGG ATTGCTCGAG 720
CCCAGGAGTT CGAGACCAGC CTGGGCAACA TAGTGAGACT CCGTCTCTCC AAAAAAAAAA 780
TAAAGTTAGC ATGGTGTGGT GGTGCGCACC TGTGGTCCCA GCATTTGAGA AGCTGAGGTC 840
GGAGGGTTGC TTGATCCTGG AAAGTCAGGG CTGCAGTGAG CCATACTCCA ACCTGGGTGA 900
CAGAGCAAGA CTCTGTCTGT CTCTTTGGGA AAAAAAAAAA ATCCAACTTA CGAGTTCTCT 960
TGTGCTCCCT CTCCACTGTT CCTCTTTGCT CTTTCATCCC TCCTGACTCC AGAAGAGGGC 1020
TCTACCACTC GCTGCTAATG CCTTCACATT TGTCTGGATT CCTGCCTCCT GGGGACCTCA 1080
TCCTTGCCAG CCCCTGTTGC TGTGCCTGTG CCCTACCAGG GGTGTTTTCA TGTTCTCATC 1140
AGTGACCCTG CTTAGCCCTG AATATCATCA GCCGGCTCAT GCCTGACTTC TCTGTGGAGG 1200
GATTCATCCC ACGTGCATTC TTCAGGGTAT GAATCCCACA GGACCAAGAC CTTCTGGATC 1260
CCTTTCCATT TCTTCACATT CAAGAATCTC TGCAAAAGAA TGTAGCCTAA CCCCCCTAAC 1320
AATCTAAAAC TTCTTCCCAA GCACCATTTA GTGCCCCAGG ACACTTGCCT GTGGCCAGAG 1380
CGACTCTCTT CCTTTCTGCC CTTTCCATTG TCTACCCCAC CTGCCTCCCC TTTGAAAGTT 1440
GTTCAGGTTT AACTTTCCCT CCCTATTCCC TTTGTTCCCG TTTGTAGGCA GGTCTCCCTC 1500
CCCTGCAATC CCATACCATG TTCAAACAGG TTTTCTTAAA ACTCTTACAT CACTTTTCTC 1560
AGCCTACACC CCCTACTGCC CCAGACCCAA CCCCAACTCT CCCACCTCCT GTAATTTGCC 1620
CACTCCACAC ACACCCTCTG TAATGAGGCC CCTGCCCTTC AGCAGGACCT GGCTCCTGGG 1680
CTTCTTGTGG TACTTCCTGG GTATCAGCTC CCTCCAGCCT CCACCTCCAT ACCCTTCCTC 1740
TTACACTACC CCAGTCCACT AATCTCTGCT TTTTCTAGAC CTAAAATTAG AATTGTATAG 1800
ACAGCACTTA ATTCTCTTAC CTTCCCAAGC TTTCTTTTAC CTCTTACCAA GTGGTAAGCT 1860
TATGGAGTTC CCCACCCCAA CCTAGTAGTG 1890
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