EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-14883 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr22:36792780-36795730 
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: 3             
ChromosomeStartEnd
chr223679326436793883
chr223679283936793116
chr223679452036794572
Number: 1             
IDChromosomeStartEnd
GH22I036394chr223679037936796045
Enhancer Sequence
GTGAGCCGAG ATCGCGCCAG TGCATTCCAG CCTGGGCGAC AGAGCGAGAC TCTGTCTCAA 60
AAAAAAAAAA AAAAAAATTA TCCAGGCATG GTGGTGTCAC ATGCCTGTAG TTCCAGCTAC 120
TCAGAAAGCT GAGGTGGAAG GATCACCTGG GCCTGAGAGA TTGAGGCTGC AGTGAGCCAT 180
GATCAGGCCA CTGCACAGTC TCAAAAAAAA AAAAAAAGAA AGAAAACAAA TGCAGAGTCT 240
GAAGATCCAG CCCAGACCCA CTGATTCTGA ATCTGCATGT TAACAAGCCC CCAGGTGGCT 300
GGCATCATAT TAAAGTGTTC AAAGCACTGG CTTAATCAGA AAGTGTCTTG TGGTTGTGCT 360
GAGGAGTTTT TAATGCATCA GACATCAGAA TCTCTAGGGA GGTTTTTTTT TAAATTTTAT 420
TTTAAGAGGC AGGGTCCCAC TCCGTCGCCC AGGTTGGAGT GCAGTGGCGC AGTCATAGCA 480
CACTGCAACC TTAAATTCCT GGGCTCAAGG AATCCTCCCA CCTCAGCCTC CCAGGAAGCT 540
AAGACTACAG GCACATGCCA TCATACCCAG CTCATTGTTT TATTTTTTTG TAGAGAATGG 600
GTCTTGCTTT GTTGCCTGGT CTGGTCTCAA ACTCCCGGGC TCAAGCAGTC CCTCTCCCTC 660
AGCCTCTAAA GTGCTGGGAT TACACACATG AGCCACCGTG CCCAACCACC TAGGGAGATT 720
TTAATTAAAC CAGTACCTCA GGTGGTGAGT CCTGAACACC CACATTTCAT ACCATTCATT 780
CAGCAAATGA TCACTGAGCA CCAGGTCTGT GCCCTCCACC TGAAGGACCA CACCTCCTCC 840
TTCCCTGGAT GGGCGCTCAG GGCCCCCTCT CTAGCGTGCA CTCAACAAAC ATTCCAGGAA 900
TCTGATGCAA TGGTTCCCGT GCCTGATTCA CAACACTGTC CATCTAGGGC TCACCCTGGT 960
CTGCATACCA TTAACACTTC CCCACTGCCC CTTGAGTCTT TGAGTGTGGT AACTCCTTCT 1020
GGAGGCCTCT CTGGATCCTG CAGCCTGGCA TGGATGTTCT CCTCTGTGGT CCCATTGTAC 1080
TTGGGGTTGC TTCTGTTTTA TGTTTTTTTG AGACACGCTC TCACTCTCTT GCCCAGACTG 1140
GAGTGTAGTC ACGTGATCTT GGCTCACTGG AGCCTTAACC TCACAGGTTC AAGTGATCCT 1200
CCTGCCTCAG CCTCCCAGGT AGCTGGGACT ATAGACACGT GCTACTACAG TCAGCTAATT 1260
TATTTTTCGT AGAGATGGGG TCTTTCTATA CGGCCCATGC TGATCTCAAA CTCTTAGCCT 1320
CAAACAATCT TCCTGCCTCA GCCTCCAAAA GTGCTTGGAT TAGAGTCAAG GCCACCCCAC 1380
CTGGCCTTAG GGTTGCTTCT GTCGTAGCAT TCTCATGCTG TCAGCTTGCC TACCCCTGGA 1440
CAAGGAGGTC ATGAGCTTCC TAAAGACAGA CGAGTGCTTT ATGCTTATAT CCCAAGTACA 1500
TGGCACGGAA CCTAGCACTC TGCAAGACCC TCAATAAATG TCCATGGCAT GAATAAACAA 1560
ATAAGCTACT AAATTGAAAT AAGAATCTAT GTGGGCTGGG CACGGTGGCT CACAGCTGTA 1620
ATCCCAGCAC TTTGGGAGGC CTAGGCAGGC AGATCATTTG ATCCCGAGTA GCTGGGACTA 1680
CAGGTGCCCA CCACCACACC CAGCTAATTT TTTGTATTTT TTAGTAGAGA CGGGCTTTCA 1740
CTGTGTTAGC CAGGATGGTC TCGATCTCTG ACCTCGTGAT CCGCCCACCT TGGCCTCCCA 1800
AAGTGCCAGG ATTACAGGTG GGAGCCACCG CACCCAGCCC ATGCTTCTGT TTTTTTAAAC 1860
AGCGTTATTG GGATAAAATT CACACACCTT ACAACTCAGT TGTTTTTAGT ATATTCACAG 1920
AGCTGTGCAG TCATGACCAG TAATTCCTGA ACATTTTCAT CACCCTAAAG AAACTCCATA 1980
TCCATGAACA GTCACTTCCT GTTTTCCCTC AGCCTCCTCC CCCAGCGCTA GGCAACCATT 2040
AATCTACCTT CTGACTCTAC AGATAATTTG CCTATTGTGG ACATTCCGTA TAAATGGAAT 2100
CATACAATAT GTGATCTTTT GTGTCTGGCT TCTTTGATCT AGCATGATGA TTTCAGGGTT 2160
CATCCATGTC GTAGCATCTA TCAGTATTTC ATTCCTTTCT ATTGCCGAAT GCCATTTCAT 2220
TGTATGGATA AGCTACATTT CATTGATTCA TTCATCAGAT AATAACGAAC CTTCCCGCAG 2280
GTGTACAGCA TTTGGCTTTT GCAATAGCAT TTTCATGCCA CCTCGCTTCA TCTTGATGTT 2340
TACTGTTTGA GGAGGGTTGT GTTTAGCCCC ATTTTGCAGA TGAGTGAACT GAGGCCAGAG 2400
TGAGCCGTTG TGACTTGCCA CAGAGATCAC AAGGCTATTA AATAGCAGAG TCATAACTCG 2460
AAACCCTTTT CTCTGTGCCA TTCTGCCTCC CTCCCCAATC CAACTCATGG CACATGTCTC 2520
TTTTCCCCTC ATACACCCAC TATTCATGGT GTCCACCGTG CCCTATGGCC ACCTGAACTT 2580
GGATACACAG AGGTTTGGGT GTGTGCTCTG GGAGGGTGTC AAGCCCTTAT CTGATCTGGA 2640
TTTCTAGGCC AAAGTTCAGC CTTCCAGCCT GAGTGCATGC AGGTCACTTC TGGGTCCCAG 2700
ATGTGGGTAG GTGGGGTATA GCCAAGAGGA ACCCCACAGC TCAGGAATCC ATCAGACCTC 2760
ACCATCCACT CTGCAGAAAA GGGACCTCTC CCACCTGCCC CAGTGCCACC CAGCTCTTCC 2820
GATCGCCACT TCCTTCTGCT TGACCCTTCT TGCCACACCC TTTCCTCTCC AACCACAAAG 2880
AACTTTAAAC ACACTTCTTT TATGGCACTT GCCATACTGG GGCATAATGA TTTTTTTATA 2940
TGTCTGCTCC 2950