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

TagContent
EnhancerAtlas ID
HS095-28800 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr7:142493970-142497020 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs57586289chr7142496164hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr7:142495587-142495607GGCGGGTGGGTGTTAGGGGG-6.06
ZNF263MA0528.1chr7:142495317-142495338GGAAGAGGGAGGGGGTGGGGA+6.67
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_02778chr7:142493717-142496872Astrocytes
SE_10458chr7:142493711-142499724CD19_Primary
SE_10992chr7:142490229-142511921CD20
SE_11861chr7:142491838-142509385CD3
SE_14462chr7:142491771-142511449CD4_Memory_Primary_7pool
SE_15402chr7:142491881-142500323CD4_Memory_Primary_8pool
SE_15813chr7:142491658-142500550CD4_Naive_Primary_7pool
SE_16301chr7:142491721-142501237CD4_Naive_Primary_8pool
SE_16869chr7:142491830-142509475CD4p_CD225int_CD127p_Tmem
SE_17317chr7:142490561-142513566CD4p_CD25-_CD45RAp_Naive
SE_17799chr7:142490662-142511579CD4p_CD25-_CD45ROp_Memory
SE_18273chr7:142490551-142512240CD4p_CD25-_Il17-_PMAstim_Th
SE_19176chr7:142492574-142509454CD4p_CD25-_Il17p_PMAstim_Th17
SE_19996chr7:142490747-142509282CD56
SE_20831chr7:142492309-142500862CD8_Memory_7pool
SE_21462chr7:142491654-142509656CD8_Naive_7pool
SE_21921chr7:142491616-142509527CD8_Naive_8pool
SE_22327chr7:142490622-142510498CD8_primiary
SE_25347chr7:142493902-142514183DND41
SE_30895chr7:142491858-142516124Fetal_Thymus
SE_39429chr7:142493774-142509301Jurkat
SE_49938chr7:142494048-142506653RPMI-8402
SE_50773chr7:142493655-142498088Sigmoid_Colon
SE_53139chr7:142493705-142500292Small_Intestine
SE_55099chr7:142493654-142508314Thymus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr7142494676142496039
chr7142496464142496800
Number: 1             
IDChromosomeStartEnd
GH07I142798chr7142495885142497684
Enhancer Sequence
GGGGGCGGAC CCATGGGAGG GGCTGTTTTT GTACAAAGCT GTAACATTGT GGGGACAGGG 60
TCCCTAGCGG GCCAGAAACT CCTACAATGA GCAGTTCTTC GGGCCAGGGA CACGGCTCAC 120
CGTGCTAGGT AAGAAGGGGG CTCCAGGTGG GAGAGAGGGT GAGCAGCCCA GCCTGCACGA 180
CCCCAGAACC CTGTTCTTAG GGGAGTGGAC ACTGGGCAAT CCAGGGCCCT CCTCGAGGGA 240
AGCGGGGTTT GCGCCAGGGT CCCCAGGGCT GTGCGAACAC CGGGGAGCTG TTTTTTGGAG 300
AAGGCTCTAG GCTGACCGTA CTGGGTAAGG AGGCGGTTGG GGCTCCGGAG AGCTCCGAGA 360
GGGCGGGATG GGCAGAGGTA AGCAGCTGCC CCACTCTGAG AGGGGCTGTG CTGAGAGGCG 420
CTGCTGGGCG TCTGGGCGGA GGACTCCTGG TTCTGGGTGC TGGGAGAGCG ATGGGGCTCT 480
CAGCGGTGGG AAGGACCCGA GCTGAGTCTG GGACAGCAGA GCGGGCAGCA CCGGTTTTTG 540
TCCTGGGCCT CCAGGCTGTG AGCACAGATA CGCAGTATTT TGGCCCAGGC ACCCGGCTGA 600
CAGTGCTCGG TAAGCGGGGG CTCCCGCTGA AGCCCCGGAA CTGGGGAGGG GGCGCCCCGG 660
GACGCCGGGG GCGTCGCAGG GCCAGTTTCT GTGCCGCGTC TCGGGGCTGT GAGCCAAAAA 720
CATTCAGTAC TTCGGCGCCG GGACCCGGCT CTCAGTGCTG GGTAAGCTGG GGCCGCCGGG 780
GGACCGGGGA CGAGACTGCG CTCGGGTTTT TGTGCGGGGC TCGGGGGCCG TGACCAAGAG 840
ACCCAGTACT TCGGGCCAGG CACGCGGCTC CTGGTGCTCG GTGAGCGCGG GCTGCTGGGG 900
CGCGGGCGCG GGCGGCTTGG GTCTGGTTTT TGCGGGGAGT CCCCGGGCTG TGCTCTGGGG 960
CCAACGTCCT GACTTTCGGG GCCGGCAGCA GGCTGACCGT GCTGGGTGAG TTTTCGCGGG 1020
ACCACCCGGG CGGCGGGATT CAGGTGGAAG GCGGCGGCTG CTTCGCGGCA CCCGGTCCGG 1080
CCCTGTGCTG GGAGACCTGG GCTGGGTCCC CAGGGTGGGC AGGAGCTCGG GGAGCCTTAG 1140
AGGTTTGCAT GCGGGGGTGC ACCTCCGTGC TCCTACGAGC AGTACTTCGG GCCGGGCACC 1200
AGGCTCACGG TCACAGGTGA GATTCGGGCG TCTCCCCACC TTCCAGCCCC TCGGTCCCCG 1260
GAGTCGGAGG GTGGACCGGA GCTGGAGGAG CTGGGTGTCC GGGGTCAGCT CTGCAAGGTC 1320
ACCTCCCCGC TCCTGGGGAA AGACTGGGGA AGAGGGAGGG GGTGGGGAGG TGCTCAGAGT 1380
CCGGAAAGCT GAGCAGAGGG CGAGGCCACT TTTAATCTTT TTTCTGGGGT GTTTAGAGAG 1440
AAGGTGAACG ATGGAGGAGA GGATTTGTTA GGACTCTGGG AGAGGCGAGA CTGGAGAGGA 1500
CGAAGGGAAA TCCTGGTTTG GGGAATGGGT AGGAGTGGGG GTAACTGCTA TTCGTAGGCA 1560
AAAAGAGCTG AGCAGGCTGG GAACAGCGCG GGTGGGCAAG GGTCAGCACT GCGGGCAGGC 1620
GGGTGGGTGT TAGGGGGCAG AAATCCTGCA GCCGAGGGTG CAGTAGAACA CAGAAGAAAA 1680
AGCCTGCCAA ACAAAAGTGG AACAGAGAAG CCAAAAAGGG AGATGAACAT GAGTCAGTGA 1740
AGAAAAGAAT GAAAGTTTAC TGTTTAGCAG TGTGGATCTC TAATCCGACT TAAAACTCCT 1800
TGTTCCCGAT TCCTATTCCT CCTAAGCCAG AGATCCCTGG GTCCAGGGTG AGGGCACGGC 1860
ATTCATGCTT ACCCACGGGC TGGTCAACAA AGAGGTGCTG ACCTGAGAGT AGGGCACATA 1920
ACCTCAGCCA CTGGGGTACA CTTACCACCC CCGCCCCCGT GTAGCTCCCT CCCCTATCCT 1980
GAAATCTCCC TTAGCACACT AAGTATTCTA GGTTAAACAG CCCAGATGTT CAGGGAGTTC 2040
ATTCGCCACA AACACACATT AAAATGCAGA CAATTTGCCT GTGAGATGAG GAAAATTCTC 2100
TGGAAGATTT AGGCCCTGAG AGCTGAAAAG GGACCCTAAA CATTACCTGG TGACAACTGC 2160
CCTGAGGCCA GAGAAGAGAA CTCACAATAT TGGTATATTA ACCGGTACCA TTTGTAGTTA 2220
GGCTGTCATT AATCTGGGTG TAATGGGGCT CAGCTACAGA GAAGCGTATC CAGAGGAAAT 2280
GTGGGGTTCC TGCAGTCAGC TGGGGCACCG AAAAGACCCA GACTTTAGAA CCAGATAAAG 2340
GCTGAGTTCG AACCTCTGGT TCTTTTGTGA TGTGGTGACC TTGGGCAAAT TAATGTGTGA 2400
ACCTCAGTTT CCTCAACTAT AAAATGTAAT GAACAATACC TACCACTTAC TATTGCTGTG 2460
AGGAAGAAAA GAGAGTCAAC ATGTACCGTG TACAGATTAT TGATGTAATT CAATGGTTCT 2520
TTTCCCCATC CTCCTAGGAG GTCACTGGGG AGACAGGGGG CAGGGTCAGC CCAGTGCCAA 2580
AGGATGGGCA GGATCTGAAG TGTGGAAATG GAGTAAGGCT GTGTCTGTGT CAGAGGTGGG 2640
TTGGGAAGAT GTGAGACAAA CATCACAATT TTGCCTAAGG TGAATCCAAC CCACAAGTAG 2700
AGCACAGGCC AACAGCAGCT CACTAGTACA CATACTTACA CCAGCAGCTC ACTAGTACAC 2760
ACACTTACAC CAGACGCTCA CTGGTACACA CTCACACCAG AAGCTCATTA GAACACACAC 2820
ACCGTCAGCT TGCTAGTACA CACACTTACA CCAGAAGCTC ACTAGTATAC ACTTACACCA 2880
GAAGCTCACT AGTACACACA CTTACTCCAG AAGCTCACTA GTACACACAC TTACACCCAC 2940
AGAGACAAGC CCCACACCAC ACGGACTCAC AAATGCAGAA GAAGAGTTGA CCCTGCCCTC 3000
ATGTACAGAT AGTATGCTGG TGTGTAGTGA GAGGCGGCTA GTGTTCGCCA 3050