EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-53195 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr22:36792980-36795640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs113283142chr2236793192hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE40MA0464.2chr22:36793927-36793937GTCACGTGAT-6.02
IRF1MA0050.2chr22:36792986-36793007AAAAAAAAAAAGAAAGAAAAC-6.33
LMX1BMA0703.2chr22:36793497-36793508ATTTTAATTAA+6.62
MITFMA0620.2chr22:36793923-36793941TGTAGTCACGTGATCTTG+6.39
MITFMA0620.2chr22:36793923-36793941TGTAGTCACGTGATCTTG-6.39
TFEBMA0692.1chr22:36793927-36793937GTCACGTGAT-6.02
ZEB1MA0103.3chr22:36795569-36795580CCCACCTGCCC+6.14
ZNF263MA0528.1chr22:36794782-36794803TTTCCCTCAGCCTCCTCCCCC-6.35
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_02243chr22:36792803-36795746Astrocytes
SE_09195chr22:36793283-36794515CD14
SE_09195chr22:36794625-36796097CD14
SE_23071chr22:36793270-36794505Colon_Crypt_1
SE_23071chr22:36794537-36795940Colon_Crypt_1
SE_23740chr22:36794031-36794414Colon_Crypt_2
SE_23740chr22:36794917-36795925Colon_Crypt_2
SE_24731chr22:36794523-36795952Colon_Crypt_3
SE_27650chr22:36794920-36795891Fetal_Intestine
SE_28644chr22:36794893-36795996Fetal_Intestine_Large
SE_31378chr22:36795072-36795714Gastric
SE_35832chr22:36792965-36794595HMEC
SE_35832chr22:36794732-36795751HMEC
SE_37948chr22:36792951-36796119HUVEC
SE_42094chr22:36793117-36794471Lung
SE_42094chr22:36794971-36795789Lung
SE_45604chr22:36791159-36795983Osteoblasts
SE_50050chr22:36794528-36795984Sigmoid_Colon
SE_52340chr22:36794806-36796029Small_Intestine
SE_53283chr22:36794991-36796001Spleen
SE_58448chr22:36724049-36832686Ly1
SE_62151chr22:36773097-36852649Toledo
SE_64824chr22:36793272-36794626NHEK
SE_64824chr22:36794653-36795676NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223679326436793883
chr223679452036794572
Number: 1             
IDChromosomeStartEnd
GH22I036394chr223679037936796045
Enhancer Sequence
TCAAAAAAAA AAAAAAAGAA AGAAAACAAA TGCAGAGTCT GAAGATCCAG CCCAGACCCA 60
CTGATTCTGA ATCTGCATGT TAACAAGCCC CCAGGTGGCT GGCATCATAT TAAAGTGTTC 120
AAAGCACTGG CTTAATCAGA AAGTGTCTTG TGGTTGTGCT GAGGAGTTTT TAATGCATCA 180
GACATCAGAA TCTCTAGGGA GGTTTTTTTT TAAATTTTAT TTTAAGAGGC AGGGTCCCAC 240
TCCGTCGCCC AGGTTGGAGT GCAGTGGCGC AGTCATAGCA CACTGCAACC TTAAATTCCT 300
GGGCTCAAGG AATCCTCCCA CCTCAGCCTC CCAGGAAGCT AAGACTACAG GCACATGCCA 360
TCATACCCAG CTCATTGTTT TATTTTTTTG TAGAGAATGG GTCTTGCTTT GTTGCCTGGT 420
CTGGTCTCAA ACTCCCGGGC TCAAGCAGTC CCTCTCCCTC AGCCTCTAAA GTGCTGGGAT 480
TACACACATG AGCCACCGTG CCCAACCACC TAGGGAGATT TTAATTAAAC CAGTACCTCA 540
GGTGGTGAGT CCTGAACACC CACATTTCAT ACCATTCATT CAGCAAATGA TCACTGAGCA 600
CCAGGTCTGT GCCCTCCACC TGAAGGACCA CACCTCCTCC TTCCCTGGAT GGGCGCTCAG 660
GGCCCCCTCT CTAGCGTGCA CTCAACAAAC ATTCCAGGAA TCTGATGCAA TGGTTCCCGT 720
GCCTGATTCA CAACACTGTC CATCTAGGGC TCACCCTGGT CTGCATACCA TTAACACTTC 780
CCCACTGCCC CTTGAGTCTT TGAGTGTGGT AACTCCTTCT GGAGGCCTCT CTGGATCCTG 840
CAGCCTGGCA TGGATGTTCT CCTCTGTGGT CCCATTGTAC TTGGGGTTGC TTCTGTTTTA 900
TGTTTTTTTG AGACACGCTC TCACTCTCTT GCCCAGACTG GAGTGTAGTC ACGTGATCTT 960
GGCTCACTGG AGCCTTAACC TCACAGGTTC AAGTGATCCT CCTGCCTCAG CCTCCCAGGT 1020
AGCTGGGACT ATAGACACGT GCTACTACAG TCAGCTAATT TATTTTTCGT AGAGATGGGG 1080
TCTTTCTATA CGGCCCATGC TGATCTCAAA CTCTTAGCCT CAAACAATCT TCCTGCCTCA 1140
GCCTCCAAAA GTGCTTGGAT TAGAGTCAAG GCCACCCCAC CTGGCCTTAG GGTTGCTTCT 1200
GTCGTAGCAT TCTCATGCTG TCAGCTTGCC TACCCCTGGA CAAGGAGGTC ATGAGCTTCC 1260
TAAAGACAGA CGAGTGCTTT ATGCTTATAT CCCAAGTACA TGGCACGGAA CCTAGCACTC 1320
TGCAAGACCC TCAATAAATG TCCATGGCAT GAATAAACAA ATAAGCTACT AAATTGAAAT 1380
AAGAATCTAT GTGGGCTGGG CACGGTGGCT CACAGCTGTA ATCCCAGCAC TTTGGGAGGC 1440
CTAGGCAGGC AGATCATTTG ATCCCGAGTA GCTGGGACTA CAGGTGCCCA CCACCACACC 1500
CAGCTAATTT TTTGTATTTT TTAGTAGAGA CGGGCTTTCA CTGTGTTAGC CAGGATGGTC 1560
TCGATCTCTG ACCTCGTGAT CCGCCCACCT TGGCCTCCCA AAGTGCCAGG ATTACAGGTG 1620
GGAGCCACCG CACCCAGCCC ATGCTTCTGT TTTTTTAAAC AGCGTTATTG GGATAAAATT 1680
CACACACCTT ACAACTCAGT TGTTTTTAGT ATATTCACAG AGCTGTGCAG TCATGACCAG 1740
TAATTCCTGA ACATTTTCAT CACCCTAAAG AAACTCCATA TCCATGAACA GTCACTTCCT 1800
GTTTTCCCTC AGCCTCCTCC CCCAGCGCTA GGCAACCATT AATCTACCTT CTGACTCTAC 1860
AGATAATTTG CCTATTGTGG ACATTCCGTA TAAATGGAAT CATACAATAT GTGATCTTTT 1920
GTGTCTGGCT TCTTTGATCT AGCATGATGA TTTCAGGGTT CATCCATGTC GTAGCATCTA 1980
TCAGTATTTC ATTCCTTTCT ATTGCCGAAT GCCATTTCAT TGTATGGATA AGCTACATTT 2040
CATTGATTCA TTCATCAGAT AATAACGAAC CTTCCCGCAG GTGTACAGCA TTTGGCTTTT 2100
GCAATAGCAT TTTCATGCCA CCTCGCTTCA TCTTGATGTT TACTGTTTGA GGAGGGTTGT 2160
GTTTAGCCCC ATTTTGCAGA TGAGTGAACT GAGGCCAGAG TGAGCCGTTG TGACTTGCCA 2220
CAGAGATCAC AAGGCTATTA AATAGCAGAG TCATAACTCG AAACCCTTTT CTCTGTGCCA 2280
TTCTGCCTCC CTCCCCAATC CAACTCATGG CACATGTCTC TTTTCCCCTC ATACACCCAC 2340
TATTCATGGT GTCCACCGTG CCCTATGGCC ACCTGAACTT GGATACACAG AGGTTTGGGT 2400
GTGTGCTCTG GGAGGGTGTC AAGCCCTTAT CTGATCTGGA TTTCTAGGCC AAAGTTCAGC 2460
CTTCCAGCCT GAGTGCATGC AGGTCACTTC TGGGTCCCAG ATGTGGGTAG GTGGGGTATA 2520
GCCAAGAGGA ACCCCACAGC TCAGGAATCC ATCAGACCTC ACCATCCACT CTGCAGAAAA 2580
GGGACCTCTC CCACCTGCCC CAGTGCCACC CAGCTCTTCC GATCGCCACT TCCTTCTGCT 2640
TGACCCTTCT TGCCACACCC 2660