| Tag | Content |
|---|
EnhancerAtlas ID | HS116-15379 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:73683760-73686140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr17:73685565-73685576 | TGCTTTGTTTT | - | 6.02 | | SPI1 | MA0080.4 | chr17:73685165-73685179 | TACTTCCTCTTTCC | - | 6.51 | | SPIC | MA0687.1 | chr17:73685165-73685179 | TACTTCCTCTTTCC | - | 6.91 | | ZNF263 | MA0528.1 | chr17:73683781-73683802 | CTCCCCACCTTCTCCTGCCCC | - | 6.26 | | ZNF263 | MA0528.1 | chr17:73684262-73684283 | GGTGCAGAAAGGGGAGGAAGA | + | 6.52 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_03279 | chr17:73683982-73685223 | Brain_Angular_Gyrus | | SE_03279 | chr17:73685354-73686038 | Brain_Angular_Gyrus | | SE_04001 | chr17:73682465-73705208 | Brain_Anterior_Caudate | | SE_05218 | chr17:73683487-73704230 | Brain_Cingulate_Gyrus | | SE_06028 | chr17:73679436-73705327 | Brain_Hippocampus_Middle | | SE_07212 | chr17:73682397-73698116 | Brain_Hippocampus_Middle_150 | | SE_08211 | chr17:73682578-73702695 | Brain_Inferior_Temporal_Lobe | | SE_23597 | chr17:73684055-73684650 | Colon_Crypt_1 | | SE_24278 | chr17:73684079-73684616 | Colon_Crypt_2 | | SE_26294 | chr17:73683489-73686041 | Duodenum_Smooth_Muscle | | SE_26940 | chr17:73683620-73687341 | Esophagus | | SE_28154 | chr17:73683929-73684707 | Fetal_Intestine | | SE_31090 | chr17:73682484-73690062 | Fetal_Thymus | | SE_31632 | chr17:73683706-73685738 | Gastric | | SE_33907 | chr17:73683601-73687045 | HCC1954 | | SE_34296 | chr17:73683666-73684693 | HCT-116 | | SE_34660 | chr17:73683810-73686071 | HeLa | | SE_35907 | chr17:73679249-73694632 | HMEC | | SE_38365 | chr17:73679204-73691897 | HUVEC | | SE_41082 | chr17:73683616-73685924 | Left_Ventricle | | SE_42678 | chr17:73683523-73686080 | Lung | | SE_49201 | chr17:73683603-73685243 | Right_Atrium | | SE_50776 | chr17:73683659-73686106 | Sigmoid_Colon | | SE_52592 | chr17:73683710-73686039 | Small_Intestine | | SE_53680 | chr17:73683550-73686129 | Spleen | | SE_55482 | chr17:73683668-73688641 | Thymus | | SE_56442 | chr17:73684070-73685371 | u87 | | SE_56442 | chr17:73685734-73692981 | u87 | | SE_59560 | chr17:73656917-73686758 | Ly3 | | SE_64300 | chr17:73679247-73688655 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 73685500 | 73685825 | | chr17 | 73684115 | 73686035 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I075683 | chr17 | 73679125 | 73698792 |
|
Enhancer Sequence | GTAATTCAGC GTTGGTGTCC CCTCCCCACC TTCTCCTGCC CCTTGGCAGA CTTTTATTGC 60
AAGCCTAGCC CTTTTGTTAG CTGCTCTTCT GCTGCCTGTC CGTCTGACAT TTCTAGTGAA 120
TCTACACATG AAACTCACTG TGGAGTTGAC CAGGCTGGGA GTCTGAAGTT AAAACATAAC 180
AGCTGAAGGT AGGTGTGGAA CCTAAACTTG ACAGAAGACA AACTGACAGT GTTTGGGGTG 240
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGAGAG AGACAGAGAG AGGTCAGTGC 300
TTGAGCACCT TCTGTGGACC AGGCTGACTA TTAGACTTGG TGATTTTTGT GAGTACACAG 360
AGTAGAGTAG TTTGTCTTCA TCGGCCAGGT GAGCATGAGG GTAGAGGAAG GCTTCCCTGG 420
GCTGGGCTGA GGCCTACACG GGGCTTTCTA GGCAGGAGTG GGGAGAAGGT GATTTCAGGG 480
AGCAGGCATT GCAAAGATCC TGGGTGCAGA AAGGGGAGGA AGAGGCTGAA ATGGGCAGCA 540
GGGAATCCTC AAGGCTCGTG GGCCACAGTG AGGATCTGTT TTTAAGGAGC TATTGTGCTC 600
GTGAAGTGAG ATCTCATCAG GCCATGGGCT GTCCCAGGTC TGAGAGAATA AAGGTTTGAA 660
AGGAGTCATT TTACTAATCT GCCTCCCTAG CTGCCACGTA CTTGTAAGAT GCAAGATTAC 720
ATTGCCCAAC AGGAAACCCC CAGTCTGTAG CATTCTTGCC TGTGGCCTCG GGGCTGGCTG 780
CCCTGTGCCC CTGTTCAGAG TGCTTTCTCT GTGCCCGCTA CTCCCGAAGC TGGAAAGAAA 840
ACATGACGTT TAGATTTGGT GGGATCTAGA TGCTGGCGGC TGCCTTTGTG GAACTCAAGT 900
TTGACACTGG AGCTTTGTGG GGCCGGTTCC AGGAAGGATT GAGGAAGCAT TGTTGGCTGT 960
AAATAAACCT CCATTCTCTT ACTCAGGACT TGGTACTTCT CTGCTGAGTA AATCCTCCCA 1020
GCTCAAATGG CAGCTTGTCC AGTTTCGTGG GTCTATATTG TTGTTACTTC CTTCCTGCGC 1080
TCCAGTCAGC TTCATCAATG GCTGGACTTT TGTATTCTCT GCAGGAGGAA CCATATTCCA 1140
GGTTCTGTAA TTCTTGAGAA CCAGGCCCCT GCCACTGACC TACAGTTGCA TCTTCCAAGT 1200
CTCAGTCACA GTTGGTTAAG AAACCAAATT GGCAGGTTGA GATCACTATT CTTCTCCAGG 1260
GACAGCGCCC AGTGTGCCGC AGCCGCCTCC TGCTCTGGTT GTTGGGCCTT TAGTCTCAGG 1320
TGGGGTCTGG GTGGATGAGG GGTGCAGGCA GAGGAGGAGA CCTCGGCTCA GATTGGTGTC 1380
CTCCACCAGC TCAGCGTTTA AACCATACTT CCTCTTTCCT CCTTTCTGTT TTCTAACTTG 1440
GCTTTTGTTT TTGTCTTTTC GTTTTTCCTT GTATCTTTTT TTTTTTTTTT TGGAGACAAT 1500
CTTGCTCTTT CAGGCTGGAG TGCAGTGGCG CAATCTCGGC TCACTGCAAC CTCCACCTCT 1560
CAAGTAGCTG GGATTACAGG CATGCACCAC CATGCCCGGC TAATTTTTGT ATTTTTAGTG 1620
GAGAGGAGGT TTTACCATGT TGTCCAGGCT GGTCCCAAAC TCCTGGCCTC AAGTGATCTG 1680
CGCACCTCAG CCTCCCAACT CCCCCAGCCT GTTTTTCCTT GTGTCTTGAT TGGAATTGAA 1740
TGAGGGGGCT GAAGAGGTGG GCCTAGTCTT TTCTCCCAGG AGCAGCCTTC CTTTCCTAGG 1800
TGAGGTGCTT TGTTTTCACC TTCCTTAGGA ACTGGGTGAA AAGCCCTCAG CCTGTTCTGG 1860
CTGTGTGTTG TTGCTCATGT CTCTGGGCTG CGGGTTCCAT GCCCTCTGGC TGATGTAGAC 1920
AGATGCCTGG TGACTAGACA TCCAGGATGA GCTCATTACT TTAACCAACT GAGAATTTCT 1980
ACCTGAAGGC CAGTGGGTGG ATTCATACGA GTCAAGACAG GTGTTTCCTG TGCATTTCAA 2040
AACGCTGCTG GCGGGGAAGA GATGAACAGT GCTTTCTTGT TGCTTTTTGC TTGTATCCTC 2100
ACAGCCCTTC TTTCCGCTTC CTGCCTCTTT AAGGGCATAG TGAGAATCTC CCCCAGAGCA 2160
GGTGGTTTAA CACCAGTGCC TTGAACGACT GGCAGTTTAA TAATCGAGCC TTTCTTCCGT 2220
CTCCTTAATT CTGTCATTTA AAATATTTCA GTGGGCGAGA GGTGACTTCT ATCAATTAAA 2280
AGATTTCAAT GGGAGGGAGG TGAGGAATGA AAAATTACCT ACCGGGTACA GTGTTCACTT 2340
TCTGGGTGAT GGGTACACTG GGAGCCCAAA CCTTACTTAT 2380
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