EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS062-00100 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr1:10751510-10753930 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs59304342chr110753094hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:10753884-10753905GAAAGAAAAGTGAAAGAGCCG-6.2
ZIC1MA0696.1chr1:10752605-10752619CCCAGCAGGGGGTG-6.06
ZIC3MA0697.1chr1:10752604-10752619GCCCAGCAGGGGGTG-6.26
ZIC4MA0751.1chr1:10752604-10752619GCCCAGCAGGGGGTG-6.02
ZNF263MA0528.1chr1:10753670-10753691CCCCCCAGCTCCTGCTCCTCT-6.25
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_23439chr1:10751268-10754639Colon_Crypt_1
SE_24212chr1:10751320-10751841Colon_Crypt_2
SE_24212chr1:10751902-10752976Colon_Crypt_2
SE_24212chr1:10753583-10755727Colon_Crypt_2
SE_25175chr1:10751275-10753513Colon_Crypt_3
SE_25175chr1:10753578-10755827Colon_Crypt_3
SE_26713chr1:10751334-10756903Esophagus
SE_28494chr1:10751152-10754734Fetal_Intestine
SE_30102chr1:10753603-10754685Fetal_Muscle
SE_31374chr1:10751200-10758378Gastric
SE_33519chr1:10752816-10756047H2171
SE_40607chr1:10741152-10758351Left_Ventricle
SE_41555chr1:10751283-10751953LNCaP
SE_41555chr1:10751958-10752993LNCaP
SE_42099chr1:10732695-10754653Lung
SE_47486chr1:10751945-10752438Pancreas
SE_47486chr1:10753613-10754480Pancreas
SE_48550chr1:10752428-10753543Psoas_Muscle
SE_48550chr1:10753580-10754631Psoas_Muscle
SE_48591chr1:10751288-10754634Right_Atrium
SE_49447chr1:10752003-10753385Right_Ventricle
SE_49447chr1:10753560-10754467Right_Ventricle
SE_54510chr1:10711383-10754578Stomach_Smooth_Muscle
SE_57180chr1:10751888-10752493VACO_400
SE_57180chr1:10753611-10754575VACO_400
SE_63296chr1:10733447-10756197NCI-H82
SE_65281chr1:10740888-10754570Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11075151610751566
chr11075180010752217
Enhancer Sequence
TCCGGGGCCG CGGGGATGTT AACCTACGAT CAGGGAGGCA TGGTGGGTCC ATGATGCCAG 60
CAGCCCTTCG AGGCCTGCGC CCCTGGCCTT GGACTATGTC AGAGAGGCCC TCGGCTGAAG 120
CTGCCCACGC TGCCCCAGAG GAAGGGACCC TCACTTCACC AGCCACGAGC CCCGGCCAGA 180
GACGAGGCCC ATGGCCCCAG CTGTATGCCG TGTGCACTAT GAAGTTGAGG GAGCTGTTCC 240
CAGCTCCTGA AGATGAGCAT GGAGTCAGCC CAGGGACCAG CTCAGAGGGG ATCTCAGCGT 300
CCTCATCTGC TTCCCTTTTT TGGTGAAGTG GGGGGAAGAC TGCTTTTCTT CTGAAGTTCT 360
GAGATTATAA GTGAAACTTC CAAGTTCAAA GAAGAGACTG AGATGGTATC ACCAGATGAC 420
TCCTCCAGGA AACAGTCAGA ACTCTGCCAC CCTGGGCCTC CCCTCTGAGT GGCCAGAGTC 480
CAGGCCTGAG TCCCACTGGG AGTGCTCTAC TCCAGCTACA GGAGGAAGCA GCTGACCTCA 540
GGGTCCCTTC TAGCTTCTAG GAAAAGTTTC CAGAGCCTGT CCCTGGAGTG CTGGGAGAAG 600
TCAGTCTCCC TAAGGCCCAG GAGAGAAGCC ACAAGAGGCT CTGCCACCTG CCTCCTACCA 660
GGGCTGGGAG GCCCTCGCTC CAGTCAGGAC ACCCTAGAGA AGGGCTTTGG AGTACTGTCC 720
CCACGACAGA CTTGGAGGGA CTGGTTGGTG GATGGCAGGA GGATGGACGC TGGCTCCAGC 780
TGGCACCCAG GTTAGGAGGA GGCCGACCAG AGGGCCTGCC TTCCAGCTCT GCAATGCCTG 840
GGTCCTGTGT GCTGGCCCAC AAGCAGAGGC TCTCCTGCCC CAGGTAAGGG GTGGTGCATT 900
GCCACCAGGC CCATCTCTGA GGTCTGCTTC TTGGCTGGGA TGGGTGGGGG CCCCATTTCC 960
GAAGAAAGGG GGTGGGGCCT GAGAGGGAGG TGATGAGACA CCGACTGGAG GTGGGGGCAG 1020
GCAGGTTCTC TGTGGGAGTG GAGGGCAGGG AGGGGCAGGG TGGCAGCCTT GGCCTTAGAC 1080
ACCTTTACCA CTTTGCCCAG CAGGGGGTGT CACACCCTTC CCGGGCGCAG AGGTCCCCAG 1140
GCCCTCCACG TCAGACCAGC CAAGATCACA CCTGGTGTCA CACAGTCCTC AAACTCTGCA 1200
AATGACACCT CCCCCCAACA AACACAGGCC CTTCTTCACC GGCCACCGTG CCACCCATCC 1260
TCATCCCCTC AGGGCTGCCT CCGGTCTCTC TGCCCACTGA CCTTTAGAAG GTCAGATATC 1320
AGCTCATGGG TCCCAAGGGC CGATGCTGTG AACTTGGGCC TATTATAAAC AACAACGCTA 1380
ACAGCCACCA GTATCACCTA TCCCATCAAT GAACCAGGAG AGTTCAGAGA TCAGTCTCAA 1440
TGAATGATCG GGCTGCTTGT TTCTTTTAAA ACATTTAAGA AGACAGCTGC TTTTGTCAAC 1500
CTAGCACGTG AGGGTCCTGG TCAAAATTTG GTTTCAATAG CCAGGGCCCA TGGGAAGCCC 1560
GCAAGAGCTG AAGGCAAAAA CACTGGAAAG AATTAGATTA AACCCAAGAA AACACCAAAA 1620
TATCAGGATA AACTGCCCCA GGTGAGCACC AGGCCTCCTG GAGCCCCCGG CCTTGTCCCA 1680
CAGGAGGCCC CCAAACCCAG ATGCCTACGT TGAGTAGTCT GTCTGGTCCA TCACCACCCC 1740
TAGGGTGGGG GCTAAAGAGG CAGGTGGGAG ACAGTCCGGG GCCCCTCACT TTGAACTGAT 1800
AACAGCCACC TCATCCCACA GATTCTCAGG TGAAAAATAC TCATTAGCCA TAATAAGCAG 1860
CTTGATCATC CGACACAGCC TTGTCCCAAA TAAATTAAAT TCCTTTACCT TGAGACAGTC 1920
GCCCCGAAAC CAGACTAACC ACCTTTCCCA ACAGGACGCT GCTTTCAAAA ACTAAACCAC 1980
CCCCCACTAA AAAAATAAAA ACACACACCC CAGAGCCAGA CACACAAAGA TCTTTGCAGA 2040
GAACAAAAAA AAAAAAAAAA AAAAAAAAAA GGCACACACA CAGAAAAAAA ACACGAAGCC 2100
ATACAAAAAA CACGGAGAAC AAAAACCCCA CAAAAACCCC CTAAATCCTC TCTCTGGGTG 2160
CCCCCCAGCT CCTGCTCCTC TCGGTTCTTT CATAATGACA AGCATCACAT TAGTCACAGC 2220
CTCTAAGCAA GTGGCAAATA ACAACAACAA CAGCCTCAGA AGTCGCCGAT CCCGAGGCCG 2280
GGACGCCGGG AGGCAGCCGC CCGACCCTCC CGGCCCCCAC CCGGCCCCGC CGCCACCTCA 2340
TTGGGCTAAA AATAAGAACT TCCGTAAAAG AAGCGAAAGA AAAGTGAAAG AGCCGCCCCT 2400
GCGTTCCCAC CGGCCGGTAC 2420