Tag | Content |
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EnhancerAtlas ID | HS095-26080 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:41698210-41700380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:41699222-41699243 | CCTTGCTTTCTCTTCCTTTTT | + | 6.23 | RREB1 | MA0073.1 | chr6:41699197-41699217 | CCCCTAACAACCCACCCCCA | + | 6.37 | RREB1 | MA0073.1 | chr6:41699928-41699948 | CCCCAGACCACCACACCCCC | + | 6.8 | RREB1 | MA0073.1 | chr6:41699196-41699216 | ACCCCTAACAACCCACCCCC | + | 6 | TFAP2A | MA0003.3 | chr6:41698610-41698621 | TGCCTCAGGCA | + | 6.02 | ZNF263 | MA0528.1 | chr6:41699230-41699251 | TCTCTTCCTTTTTCTTCCTCC | - | 6.11 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_03162 | chr6:41695324-41702122 | Brain_Angular_Gyrus | SE_03890 | chr6:41695262-41704164 | Brain_Anterior_Caudate | SE_04788 | chr6:41694181-41704406 | Brain_Cingulate_Gyrus | SE_05789 | chr6:41694011-41704397 | Brain_Hippocampus_Middle | SE_06686 | chr6:41695028-41704295 | Brain_Hippocampus_Middle_150 | SE_07757 | chr6:41694213-41702285 | Brain_Inferior_Temporal_Lobe | SE_08794 | chr6:41698649-41698904 | Brain_Mid_Frontal_Lobe | SE_10407 | chr6:41694292-41703442 | CD19_Primary | SE_10977 | chr6:41658732-41703851 | CD20 | SE_20329 | chr6:41689981-41703529 | CD56 | SE_27930 | chr6:41686945-41704088 | Fetal_Intestine | SE_28789 | chr6:41686934-41704233 | Fetal_Intestine_Large | SE_32569 | chr6:41697863-41703546 | GM12878 | SE_40921 | chr6:41697833-41699742 | Left_Ventricle | SE_48161 | chr6:41694453-41700196 | Psoas_Muscle | SE_48786 | chr6:41698203-41699142 | Right_Atrium | SE_50457 | chr6:41694581-41700186 | Sigmoid_Colon | SE_51489 | chr6:41697833-41703765 | Skeletal_Muscle | SE_53720 | chr6:41698008-41703677 | Spleen | SE_58883 | chr6:41671378-41704020 | Ly3 | SE_59865 | chr6:41670633-41703769 | Ly4 | SE_60547 | chr6:41671030-41704212 | DHL6 | SE_61043 | chr6:41671264-41704230 | HBL1 | SE_61929 | chr6:41668086-41703943 | Toledo | SE_62316 | chr6:41671424-41703890 | Tonsil | SE_65465 | chr6:41694557-41698785 | Pancreatic_islets | SE_65465 | chr6:41698849-41703616 | Pancreatic_islets |
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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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Enhancer Sequence | CTTATGGGGC CAGGTGGCTC TCCCCATAAG AAAGCTGGAC AAAAGATGGG TGGCCAGACC 60 TCATTTTTCC TCCTTAAGCC CACACTTAAG AGCCAGGAAG GAAAGCTGGT GATGACCCTG 120 CCTGTTGCCT CTGCTCCTCT TGGCTCTCAC CCACGGCTTT GCCATTTCAC AGCAAAGCAT 180 TTCCTGTGGG CATGATAAGT CCCAGATCCT ACCCTATCAC TGCGATTTTA TCTCTGTCCC 240 CAATGACATC ACAGCCAAGG GGATCTGTAT CTCTGGTGCA GTGTGGAGGA GGGACAGATG 300 ATAGGAGAGC AGGGGACAGC CACAGCTAGG AGTGCATGGT CAGTGGCCAG GCCAGATGCT 360 ACCCAGGGAA ACCCAAGTGG CAGGGCAGGG GTGGTAGAGA TGCCTCAGGC ATTGCCAAGC 420 CCCCTGCACC GTCTTATTCA ACAAGGAGAG GAGGCTGGTG TGGTGGGACA GAGAGTGGTG 480 GGAAGCCCCA CGTAAAGCAT TACATCAGAG AACATTAGAC ACATGGAGAG GCCTGTTTGC 540 AACCCATAGG TCTTTATTCC TTCCCTAGAG CTCTCCATGC CTCTATTTCC TCACTTAAGA 600 ATGAGAAATA AATAACTCAC TGAGTCATAA CAGTTCATTA GGCGCTATTC TAAGTACTAC 660 ATGTGCATCA ATATCGGCAT ACTCAGCCCT CACGACAGCA CTAGTAGGTG GGTGCTGCAA 720 GAACCCTCAC TTTTTAGGTG TGGAAACTGA GGCACAGTGG GGTTAAGCAG CTTGCCGAGG 780 CTCACACAGT GTTAAGTGGC AGAGCTGTGC AAGCCACATA GCCTGGCCCC AGAGCCCACG 840 TTCTCAACAA CCCCCTGACC AGGTGACACT GGTCCAGTGC TCAATATATA GTGGCTATGG 900 CTGTCCCAAG AAAAACTTCC TGGTTGCTTC ACCAGGACCA GTCTTTAGCT AAAGCTCAAT 960 TCTGCGGACT GCAGCATCTC CCAAACACCC CTAACAACCC ACCCCCACCA CCCCTTGCTT 1020 TCTCTTCCTT TTTCTTCCTC CCCGGTGCCT TTGGCAAAGA TTTGTAGAAG GTTCGCTTTG 1080 GAGGGAATCC CACAGATGAT CCAGATTCAC AGATATGGAA ACTGAGGCTG AACAAAGCAG 1140 AGACCTGCCC AGCCACACAG CCAGTGAGAG GCACAGTGGG GTCTCTCGAC TCCTGGTCCA 1200 GTGCTCTTAT GACTTTACTG CCGTCCCATT CTCACCCAAT GATCCCCACA GCCTCTTCTG 1260 CACATCTGAT TAAACAAGGG CCTGCTGAGG GCTGCACTGT ACGTTAATGG ACGTGGAATG 1320 CATGGCACAA AGCCGGGCAC CTAGAAGGCC ATCAGTAAGG ATGCCTCCTC CCTTCCTGGG 1380 TGTCTGGGGC TTCCAAAGAA GCCCAGGAAG TCTTGCCTGA ACCAGTCTCC TTCCCTGGCC 1440 AGTCAAGACA GGTTCCAGCC GGAGGTCCTT TGGTCACCCA TGCTGGCAGC TCAGAAGAAA 1500 GGCCAGGAAA CAGGTATGGT GCTCAGACAG GGGCCTCAGC AAGTTCCCAC CCTGCTTTTT 1560 TATTTTTATT TTTTTCATAC AAATTCTTTT TTCAATTGAG TCCAGGTCTC GCTATGTTGC 1620 CCAGGCTGGT CTCGAACTCC TGAGCTCCAG TGATCCTCCC ACCTAGGCCT CCCAAAGATC 1680 TGCTTAGAGC AGGAAACCCT GGATAGAGAA AAGAAGGTCC CCAGACCACC ACACCCCCAC 1740 CTTTTAAGAG AGAACTCCTG GGAAACCCCT TGAAGAAGTG GTCTTCTTTA GGGACTGAGA 1800 ACACAGACTT TGGAGTCAAT TGGACCTAGG TTAAAATTCC AATCCTGTCA CTTCCAGGCT 1860 GTGTGATTTT AAGTGACTTG CTTAACCTCT CTGAGTAAGT AAGTGTAATG CAAACAGTAA 1920 TTCCCACCTC ACTCTAAACA CACAATAAAT GTTGGCAACT ATTGTATAAT CAATCTTATT 1980 ATAATATTGT TCTAGTATAG CATAAAAGAA GAGATGAATA TTCTATTAAT ATAATCTTGT 2040 TTTATTGTTA CACTCTCATA GACACACATG CACAGTTCAT CTCTACCCAC ATTCCTAGAC 2100 ACTTTAACCA CACACACAAA CTCACAACCA TTACATAAAC CCCACACCAA CCCAGAAAGC 2160 AACATCATGT 2170
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