Tag | Content |
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EnhancerAtlas ID | HS059-00677 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:23893560-23894580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr1:23893803-23893817 | AAAAAAAGGAAGTA | + | 6.3 | SPIC | MA0687.1 | chr1:23893803-23893817 | AAAAAAAGGAAGTA | + | 6.79 | ZNF263 | MA0528.1 | chr1:23894480-23894501 | TTTTCCTCCACTCCCTCACCC | - | 6.11 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_01721 | chr1:23894114-23896139 | Aorta | SE_02990 | chr1:23894236-23895942 | Bladder | SE_04396 | chr1:23893786-23894682 | Brain_Anterior_Caudate | SE_06239 | chr1:23879137-23896940 | Brain_Hippocampus_Middle | SE_07293 | chr1:23893676-23896957 | Brain_Hippocampus_Middle_150 | SE_10300 | chr1:23893905-23894618 | CD19_Primary | SE_11050 | chr1:23891759-23895821 | CD20 | SE_15327 | chr1:23894282-23896070 | CD4_Memory_Primary_7pool | SE_23281 | chr1:23894157-23895276 | Colon_Crypt_1 | SE_23782 | chr1:23894110-23895236 | Colon_Crypt_2 | SE_24936 | chr1:23894139-23895632 | Colon_Crypt_3 | SE_27258 | chr1:23894169-23895985 | Esophagus | SE_27884 | chr1:23894178-23896122 | Fetal_Intestine | SE_28880 | chr1:23894076-23896000 | Fetal_Intestine_Large | SE_29676 | chr1:23894052-23896300 | Fetal_Muscle | SE_31953 | chr1:23894148-23896022 | Gastric | SE_33209 | chr1:23894237-23895252 | H1 | SE_38016 | chr1:23894037-23895844 | HUVEC | SE_41075 | chr1:23894073-23896242 | Left_Ventricle | SE_42328 | chr1:23893887-23896240 | Lung | SE_45797 | chr1:23894474-23895828 | Osteoblasts | SE_48755 | chr1:23893984-23896237 | Right_Atrium | SE_50077 | chr1:23893624-23896094 | Sigmoid_Colon | SE_52549 | chr1:23894058-23895971 | Small_Intestine | SE_53706 | chr1:23893935-23895950 | Spleen | SE_54840 | chr1:23894330-23896020 | Stomach_Smooth_Muscle | SE_55341 | chr1:23894275-23895143 | Thymus | SE_56054 | chr1:23894210-23895677 | u87 | SE_58372 | chr1:23873313-23964782 | Ly1 | SE_68324 | chr1:23879596-23905390 | TC32 | SE_68325 | chr1:23879596-23905390 | TC32 | SE_68477 | chr1:23874949-23904689 | TC71 | SE_68478 | chr1:23874949-23904689 | TC71 | SE_69046 | chr1:23893964-23895982 | H9 |
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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 |
GH01I023567 | chr1 | 23893492 | 23896026 |
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Enhancer Sequence | CGGAGCTTGC AGTGAGCCGA GATCGCAAGC CACTGAACTC CAGCCTGGGC GACAGAGCGA 60 GACTCTGTCT CAAAACAACA ACAACAACAA CATAAGTTCG CTGGACGTGG TGGCTCATGC 120 CTAAAATCCT AGCTACTCAG TAGACTGAGG CAGGAGAATC GCTTGAACCT CGGCAGTGGA 180 GGTTGCAGTG AGCCGAGATC ATGCCACTGC ACTCCAGCCT GGGTGACAGA GTGACTCCGT 240 CTCAAAAAAA GGAAGTATGT ATTTGACATG GATTTTGTTT CACAGAACTT TATGGTGTCA 300 GGCAGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT CTCAGTTTCT TTCTTTTTTT 360 GAGAGGAAGT CCCACTCTGC TGCCCAGGCT GGACTTTAGT GGCGCAATAT TGGCTCACTG 420 CAGACTCCAA CTTCCGGATT CAAGGGATTC TCCTACCTCA GCCTCCTGAG TAGCTGGGAT 480 TACAGGCGTG CGCCACCACG CCCAGCTAAT TTTTATATTT TTTGTAAAGA CGGTGTTTCG 540 CCATGTTGGC CAGGCTGGTC TCAAACTCCT GACCTCAAGT GATCCGCCCG CCTCAGCCTC 600 CCAAAAGTGC TGGGATCACA GGCGTGAGCC ACCGCGCCCG ACCTCAGTTT CTGAGTGTAT 660 TCCTACCTGA GAATATGCTG TCCACCCTTG TCTGAGTGTG GGGCTGTCCT TGGGGGCTGT 720 GCGCGGGGTG CGCCTATGTG TCTTCCTCCC TGGGTGTTTC AGCCTGCTGT GTGTGATGTG 780 TCCCCGGGTC TAGTATAGGA TCTTCCCTGG GTGTGCGGCT TTCTATGTGC GTGCTTCAGT 840 GTATGTCCAT CTTCCCCCAA TCTCCTAGCC AGGTGCGGAA CAGGGCCAAG AGGACAATAG 900 GCTCGAGCGC CCAGGTGGCC TTTTCCTCCA CTCCCTCACC CACCGCGACC CTCCCCTCCT 960 GCACCCCGCG CCCTGACTGC CCCCTCTCTG GCCCTGCCCG ACCTTCCGCG GCCCTCCCTG 1020
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