EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-12168 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr17:17588140-17590740 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:17590111-17590129GGAAGGAAAGCAGCCAGG+6.35
JUN(var.2)MA0489.1chr17:17589304-17589318ATGAGTCATCTCCC-6.96
PLAG1MA0163.1chr17:17589535-17589549CTCCCGTGGGCCCC-6.05
PPARGMA0066.1chr17:17588674-17588694AGTGGGTGATTGGGACCCAG-6.27
TCF7L2MA0523.1chr17:17589545-17589559CCCCTTTGATCTTT-6.58
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00905chr17:17588032-17590910Adrenal_Gland
SE_02900chr17:17588408-17590369Bladder
SE_03155chr17:17589036-17589522Brain_Angular_Gyrus
SE_23508chr17:17588014-17590335Colon_Crypt_1
SE_23959chr17:17588057-17590314Colon_Crypt_2
SE_24961chr17:17588069-17590283Colon_Crypt_3
SE_26187chr17:17588064-17589984Duodenum_Smooth_Muscle
SE_26567chr17:17588041-17591177Esophagus
SE_29302chr17:17588745-17589653Fetal_Intestine_Large
SE_30808chr17:17585081-17589911Fetal_Muscle
SE_31385chr17:17588024-17590346Gastric
SE_33725chr17:17587630-17591111H2171
SE_33924chr17:17587405-17591054HCC1954
SE_34327chr17:17587950-17591218HCT-116
SE_36431chr17:17584572-17591128HMEC
SE_42180chr17:17588014-17591173Lung
SE_43483chr17:17589915-17591158MCF-7
SE_45144chr17:17584844-17590535NHLF
SE_46499chr17:17584806-17590434Osteoblasts
SE_47257chr17:17585027-17592154Panc1
SE_47490chr17:17588041-17590319Pancreas
SE_48869chr17:17588041-17590415Right_Atrium
SE_50171chr17:17588038-17590837Sigmoid_Colon
SE_53329chr17:17587988-17590481Spleen
SE_54742chr17:17587966-17589914Stomach_Smooth_Muscle
SE_57229chr17:17588560-17590318VACO_400
SE_57229chr17:17590408-17590858VACO_400
SE_57532chr17:17588359-17590245VACO_503
SE_63253chr17:17584631-17604117GLC16
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr171758860017590200
Enhancer Sequence
AGGTTGGTTG TGTGGCGAAG TCCTTCAGGG CAAGTTCTGG GTTGACTCCT GGCTCCACCA 60
CATACTGAAC AGGCCATTTA CCTCTCTGTG CCTCAGTGTC CCCATCTTTA CAATCAGGAG 120
AATAACAGTA CAGACCTCAC GGTACTGAAG TAAAGATGCA GTGAGTTAAT CCATATGAAG 180
TTTAGAGCAG TGCTTTTGCC AATAAATGCT GATTGCTGCC GTCATTGTTG TATTGTTATT 240
GCTGTTCTAT CTCCATGGCA GCCCATGTTT GAAATGCATT GCTTTCCACA GCTGCCTGTG 300
GCCATGGCAT GGGTGTCTTT TTCCTCCCCT ATCCAACGTG TGGCTCCACA GGGAGGGAGG 360
AGGTGCAACA GCAACGGTGT GCGCAGAGCA GCGTCTCTGC GGGAGAGGCA CCTGGGCACT 420
GGGCCCAAGG GAACAGGGAT TTTCCAAGGA CCCACTGTTT CCAAAGTTCT GTGCTTAATG 480
TCGGGGTCCA AGCAGGAAGC ATCCCTGCAC TTGACCACAA GAAGGTCACA GCCCAGTGGG 540
TGATTGGGAC CCAGCTCATA GCCAAGGCCT CGACCAGAGC TGGAGGCTTC CTGGAGGAGG 600
GGCCTTTGAG CAGGTGCTTC AGGCACGGCG AGGTAAGAGT GAGAGGAGCA TTCCTGGCAG 660
AGGGAACACA GTGAGCAGAG CGAGTCTTTG GAAGCTGGAA GGGATGTGGC CTGTGTGCTG 720
TAGCCAAACA AGAGGGGAGG ACTTGGCTCA GAAAGAATGG TGGCGGAAGA GGTTGGGCTG 780
TTGCTGGGAC CTCCTCACTG GCCTCCCTGC CTCCATCCTG TCCCCTCCCA GGTGCTGGCC 840
AGCAGCACTG TCAGAGCGAT CGTTCTAAAC CCAGCAGATA ACCTCCAGTG GCTCCTGCTG 900
CCTTATGAAT AAAGGTCCCA TCTGTAGTTC TTCCCATGCT GTCCAGGGCC ATTTCTGGTG 960
TCCTCTGCCT GCCCTGTCCT CATTCAGTCC TGTCCCCTCC AGCCACAGCT GGCACCTCCT 1020
TGTTAAGGTG CAGCCATGTG CATCCTTGCC TCTGTGCATC GGGCTGGGCT GTTCCTTCCA 1080
CCTGGGATGC CCCTCACCTT CCTCCCTGCC GCCCCAGACC AAAACAGACG TCCTGTCTCC 1140
TCCTCCTCTG ACCTCCGAGG CAGAATGAGT CATCTCCCTT TGTCTATACT CGTGGCATAG 1200
CGTTTATCAC GGAATTATCG GCAATTCTGC CAGTGTCTGT CCTCCCCATG AGGCTGAAGC 1260
ATCGAGGCCT GAAAGCACGT CTCCTTGCTC TCTCCGGCCC AGTGCCAAGG GCGAGGCCTA 1320
GAACACAGGA CGCTCAGAAA TGCTTCCTGG CAGGAGGGCC AGGTGAGGTG GAGAGGGTGA 1380
GAGCCCCAAC ATTGTCTCCC GTGGGCCCCT TTGATCTTTA GCAAGGGCAT GCTCAGGTCT 1440
GTGTGGATCT TGTGCTGTCA GCCTTTAGAT GAGTGGGGTG AGGGGCTTGG TGGGGTCGGG 1500
GGGCAGGGGG AGGTGGCGGG CAGCTTCCCC AGGCTGCTTC CTGAGGGGGC TGGGAGAAAC 1560
TGGCTCATCC TGTTCCCCAG TGATTGAGGC AGAGCTGTGC CCTGTTCCTG GTGGGTCACT 1620
GGGGATCTGA GATTGGAATG TGACACCAGG GAAGGGGAGG CAGGGTGGGA GGCAGGGCTT 1680
GGAGGTACAG GCTGGGGCTT GGCTGGCAAA GGACAGATTT CGCTCCACTG GTTCTTGAAC 1740
CCGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGCACGCGC GCGCCGGGGA 1800
GGGGAGAGAT GGGGAAGAGA AAAACATGAG GGCAGAGAGG TGGAGTGGGG GTGGAGGACC 1860
TGGGGAGTGG TGAGCAGGGA CAGGGAGAGA TGGAAGTGGG GGGACGGCAA GGAGTGAGGG 1920
AGAAGTTCCT GCTGCTGCTG CTGGAGAGTA TGAAGAGTGT GCTTAGGGCC AGGAAGGAAA 1980
GCAGCCAGGC GCATCGTCTC ACACCACCAT CAGCCATGCC TTCCTTCGTC TGTCCAGCAG 2040
ACAACCCTAA GTGTTCTCTT GCTTGGCTCC ATGCTTGCAT GGCCCCAGAC AGGAGCAAGC 2100
CTGTGGTCCA GGCTTCGCAC CCTTGAAGTC TAGGGGCCAG GTGAACAATG AGCATCCGGT 2160
TTCTTTCTTT TTTTTGAGAT GGAGTCTTGC TCTGTCGCCC AGGCTGGAGT GCAATGGTGC 2220
GATCTCAGCT CACTGCAACC TCTGCCTCCC GGGTTCAAGC AATTCTCTGG CTCAGCCTCC 2280
CAAGTAGCTG GGATTACAGG CGCCCACCAC CACGCCCGGC TAGTTGAGCA ACCTCTTTCT 2340
GCACAAAGTG ATCAGGCTGG GGGAGAGAAG GTGCCCAGAA TGCTGTGCAG AGGCAGGAGA 2400
GGAGGGTGGA GCAGGCGAGC ATGGGGTAGG GGGCAGGGAA GCCATGTGTT AGGCACTATG 2460
GTGGGGAGCC AGGACTGCTG GGGAGTCTTC CTTTCCTCTC TGGCCTCGGT CTCATCTGTA 2520
AATGGGGGAA GAGTGGACTG CTCTTGCACT GATGGTCTGT GGACCCAAGT CACCCACTCC 2580
TTGGGCATGA GAAACCAGGG 2600