EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-09131 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr17:17613620-17616680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4924813chr1717616619hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr17:17614245-17614265GCGGGGGTGTTGATGGGGGG-6.47
SP2MA0516.2chr17:17614432-17614449AGGGAGGCGGGGCTGAG-6.07
ZEB1MA0103.3chr17:17614262-17614273GGGCAGGTGGG-6.14
ZNF263MA0528.1chr17:17614305-17614326CTCCTCCCCCTCCCCTGCTCC-6.67
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00905chr17:17612807-17614380Adrenal_Gland
SE_00905chr17:17614420-17616126Adrenal_Gland
SE_02229chr17:17612546-17615482Aorta
SE_02900chr17:17613486-17615369Bladder
SE_03155chr17:17613691-17614138Brain_Angular_Gyrus
SE_03155chr17:17614337-17615108Brain_Angular_Gyrus
SE_09034chr17:17614468-17614834Brain_Mid_Frontal_Lobe
SE_23508chr17:17613754-17615329Colon_Crypt_1
SE_23508chr17:17615584-17616165Colon_Crypt_1
SE_23959chr17:17613704-17615216Colon_Crypt_2
SE_24961chr17:17613580-17615320Colon_Crypt_3
SE_26187chr17:17614231-17616673Duodenum_Smooth_Muscle
SE_26567chr17:17612398-17616223Esophagus
SE_28394chr17:17613445-17616284Fetal_Intestine
SE_29302chr17:17610891-17616504Fetal_Intestine_Large
SE_31385chr17:17611772-17616828Gastric
SE_33924chr17:17613623-17615298HCC1954
SE_34327chr17:17611843-17615719HCT-116
SE_36431chr17:17613622-17616584HMEC
SE_38423chr17:17613171-17617849HUVEC
SE_42180chr17:17611741-17619638Lung
SE_43483chr17:17613248-17616244MCF-7
SE_46499chr17:17613461-17618930Osteoblasts
SE_47257chr17:17611677-17616484Panc1
SE_47490chr17:17613549-17614324Pancreas
SE_47490chr17:17614409-17616152Pancreas
SE_48869chr17:17614240-17616087Right_Atrium
SE_50171chr17:17612964-17616252Sigmoid_Colon
SE_53329chr17:17613684-17615214Spleen
SE_54742chr17:17613079-17616414Stomach_Smooth_Muscle
SE_63051chr17:17614295-17670945Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr171761399117616680
Number: 1             
IDChromosomeStartEnd
GH17I017708chr171761191317618634
Enhancer Sequence
CCCTTGTGGG AGCTGAGCCC CATGGAGACC CCGGGGTACC CATCCCACCC TCCAACATCC 60
ATCCCTACGT GGATATACGG CCACAGTTGC AGCTGCGGCC ATGAGGAGGG GTTTTTGCTC 120
CTTTTTAGCA GTGCTCCATC CCCCACCCCA GAGTACAGGG GGCTGCCCAG AGACCCTCCT 180
GGCCCTGGGG GCCTGTGAGT CAGAGGCTGC CAGTGGTGGC CTTTCGGCTG TTGCTGGGGA 240
AATGGCAGCA CAGTGGCCAC CAAGACTAGG ACTCCCTGGG GAGGCCCTGC TGGCCCTGGC 300
ACTGGTGGCT TGGCCTCACC CAGCCCCACC TGGCAGATGT GCCCCTTGTG GCTACCCAAG 360
GACTGGCCCC CTCCTCATTT CAGAGGTGGA GAAACTGAGG TAAAAAAGTG GAGACAGCCA 420
GGGCACCCCT CCCACAAGGC CCTGCCTCAT TTGAGACAGA GCCCTCTGGG AAGCCTGTGC 480
ATTCTGTAGG TGGGGACCTT TGGGGCCATT TTTTCCAGAG GCCCAGAGAG GGCCGTCTTC 540
TTGCCCAAGG TCACACAGCA AGTTCATGGC ATAAGCTAGC CAGCCTCGTA CTCCAGAGCT 600
CTCCTGAGGG CCCCCATGTG TCTGTGCGGG GGTGTTGATG GGGGGCAGGT GGGAGGGAGG 660
AGGTAAGGCT GATTTGTTTC CCAGCCTCCT CCCCCTCCCC TGCTCCCTTC TCTCCCTCAC 720
ACGGTTTGTT TGGAGAATGA CTCACAGGAA TGCAGCAAAA TCCTGATGGA TGGGAAGGCA 780
GGGCCGCAGT ACCCGGAAAA CCTCTCCAGG GTAGGGAGGC GGGGCTGAGC CTTGGGGCCT 840
GAGAGGCTGG TGATAGGGGA GCCCTGCATG CAGGTGGGGC GACTGAGGCC CTGGAAGAAC 900
TCTGGTCACG TCCTGGCTGG GGGTTGTCCC TCCTCGACAG AAACACACAG GCCCTGGCTG 960
CCGCAGCACC CCTGGAGCAC CCGTCCCCCA TGATTTCCAT CTTTGTGTCC CCGAGGCATC 1020
TGGTGCACTG TAGCTGACAA ACACATGCAT TTTGGCACTG AGTGTGACCC AAGTCAGACC 1080
CTCCTGTGTG TGCCCTGTCC CCCAGGTCCT CCCAGCTCCC CGGAGTTGGG GGGCGGGTGC 1140
TTGCCATTCA GTCCTTTCAG AGGCAGCCAA GGGCCTACGG CATGCTGGAC ACTGCCAGGG 1200
GCTGGGGAGG CTGGGATGGA GCTGGAGGGA AGTGGGAGGT GTACACGGGA TGGACACCTC 1260
CTGTGTATGT TCCAAATGTG CTGGAGGCCT CAACAGGTCT TGGTACAAGG TGAGGCAAAC 1320
CTTAGAGGAC CTAGGATGAA GTTTCACGTA AAGGAACAGT GGCTGTAAGG GCTCCCAGAA 1380
AGTGTAGGGA CCCTGGGAAG GTCCCAGTCT TTGAATAAAG GTGGGTGGGA CCTTATTGGT 1440
AGCTTGGGGC ATTAGGGCCC AGATATCAGG CAGCAGCATG AGGTGAGGCC CGGGCTCTGT 1500
CCCAGGGCAA GCCCTCCTCC TGCGCACCAC ATCTGGGGCC TCCGAGGAGG GACAAAGCAT 1560
TCAACTCCCG GGACCTGTGG GTGGGAATGT CCCCAGGCCC AGCCCTTTAG TGCCTGCTGA 1620
TGGCTGTCAC GCGGTGTCCG GCCCTGATGA CCAGATATGT GTTTTCAAGA GAAGCTGGAA 1680
TTTGGATTTT TATGTGAACT CTCCTGATTC TCAAATGCTG GCTCCGTTAA CAAAAGGCAC 1740
AGTGTGGTTT AAACCACACA TGTCCGCAGG CAGAGGACCA CCAGTTTCTA ATGTCTGCGC 1800
TGTGGGGCGC TTGGGTTTTT GCATTTGGTT CTTTTACATT CCTTATTTTA TTGGAAACAG 1860
CCCAAATAGT CACTGAGCTG CAACTCTGTG CTAGGTGCCG GGGCTCTATC AGCGAATAAA 1920
ACAACATGTG ACGGAGCTGC CATTTTAGTG GGAGAAGACA GTGAATAAAC ATATATCAGG 1980
TGATATGTGT TAGGAAGCAA ATGGAAGCAG GGCTCCAGAA CAGAGAGCGG CTGCAAGGCC 2040
AAGCCCACAT TTGGGTGGAA GGGGCAGCTA GTGCAAAGGC CCTGAGGTGG GGCTATGCTA 2100
GGTGTGTTAG AGGCCTGTGT GGCTGCAGCG GGAGTGGGTG GGGAAGTGGG AGGAGGTGAG 2160
GTCAGAAGGT AGCATAGGTC AAATGGCATA GGAGACTGTG GGCTGTGGTA TAAGCTTGGT 2220
TTTAAGTCTT ATGTGAGGTG GGAGCCATGG AGGATTCCTA GGGAGGGAGG GTCAGGATCA 2280
GACTTGGTTT AACAGGCTCT GTCTGGGTGT TGTAATGGCT GAGTGGGGCA AGGATGGGCC 2340
TAGGAGGCCC AGAAGGGGCT ATTGCACTTG TCTGGCTGAG TGATGATGCG GCCTGAACAG 2400
GAAGGGGGTA GTCACCAGAG GGTGACCTGA GGAAACTGTG GTCAAGCCTC TCCATGGTGT 2460
AAACAGTAAA CACGATACTG ATTCTAAGGA CTTGGTAGTA ACATGGAAAT GGTGACTGTG 2520
TATAATGCTA TGTGAAAATA GGATTAGAAA ATTGTACATT AAAAACACAC CAGCCCAGAT 2580
GCAAAAGGCT GCAGATCATA TGATTCCATT CATACGAAAT GCCCAGGACA GGCGAATCCA 2640
GAGAGACAGA CAGGAGGTGA GCAATTGCCA GGGGCTGGGG GTGGGGAAAT GGGGGGTGAC 2700
TGCCTATGGG AACAGGTTTC TTTTTGGGAG GGGGATGAAA ATGTTCTGAA ATTAGGTAGC 2760
AGTGATAGTT GCACAACTTC ATGAATATAC CAAAACCCTG AGTTGTCCCC TTTAAAAGGG 2820
TGAATTTTAT AGTGAGTGAA TTATACCTCA AAAAAAAAAT TTTTTTTAAG GCATGTCCAG 2880
ATTTCTAACC AAAATTGGAT GCACATAGAA AACATTGCAA GGAGCTGGGC GTGATGGTGC 2940
CTGTGGTCCC CACTGCTTGG GAGGCCAAGG CAGGTGAATC ACCTAAGCCC AGGAGTTCAA 3000
GACTAGAGCC TGGGTGATAT AGTGAGATCC TGTCTCTAAA TAATAATAAT AGGCCAGCTG 3060