EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS138-12421 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr14:55573520-55576310 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr14:55575108-55575119GATGAGTCACC-6.32
IRF1MA0050.2chr14:55576267-55576288GTCCAGTTTCAATTTCTTTAT+6.01
JUNDMA0491.1chr14:55575108-55575119GATGAGTCACC-6.62
ZNF263MA0528.1chr14:55575036-55575057GGAGGAGGGCGAGGGGAGAGG+7.74
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00244chr14:55563236-55576350Adipose_Nuclei
SE_00820chr14:55574748-55575102Adipose_Tissue
SE_02600chr14:55573844-55576160Astrocytes
SE_09388chr14:55568067-55576360CD14
SE_23110chr14:55574129-55575416Colon_Crypt_1
SE_23790chr14:55574594-55575269Colon_Crypt_2
SE_24786chr14:55574109-55575428Colon_Crypt_3
SE_26013chr14:55573672-55575878Duodenum_Smooth_Muscle
SE_26711chr14:55573567-55575917Esophagus
SE_27630chr14:55573899-55576071Fetal_Intestine
SE_28543chr14:55573873-55576230Fetal_Intestine_Large
SE_31668chr14:55574018-55575868Gastric
SE_33558chr14:55573897-55579764H2171
SE_34039chr14:55574107-55575498HCC1954
SE_34802chr14:55573592-55576155HeLa
SE_36310chr14:55573891-55575863HMEC
SE_37768chr14:55573433-55575974HSMMtube
SE_41170chr14:55573962-55575665Left_Ventricle
SE_42472chr14:55573658-55575611Lung
SE_44570chr14:55573874-55576148NHDF-Ad
SE_45117chr14:55573558-55575933NHLF
SE_46036chr14:55573692-55576091Osteoblasts
SE_46880chr14:55574151-55574573Ovary
SE_46880chr14:55574627-55575401Ovary
SE_49010chr14:55574074-55575920Right_Atrium
SE_50181chr14:55574075-55575919Sigmoid_Colon
SE_52430chr14:55573656-55575984Small_Intestine
SE_56717chr14:55573869-55576081u87
SE_57551chr14:55574279-55575356VACO_503
SE_64542chr14:55574036-55575714NHEK
SE_66903chr14:55573897-55579764H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr145557426455575347
chr145557446555575376
Number: 1             
IDChromosomeStartEnd
GH14I055097chr145556377555576469
Enhancer Sequence
ATAGATTGAC TTTATGAGAA GTGAATGCTA AATGAATTTT AACTTAAATG TAGATTCATA 60
AATTATTTCT TTTGTGTTTT TATCTTTTAT TGTTTTTTGA GACAGAGTCT CACTCTGTTG 120
CCCAGGCTGG AGTACAGTGG CTTGATCTCG GCTCACTACA ACCTCCACCT CCTGGTTCAA 180
GTGATTGTCC TGTCTCACCC TCCCCAGTAA CTGGGATTAC AGGCGCCCAC CACCACACCC 240
AGGTAATTCT TGTGTTTTTG TAGAGGTGGG GTCTCGCCAT GTTGTCCAGG CCGGTCTGGA 300
ACTCCTGGCC TCAAGCGATC TGCCCGCCTC AGCCTCCCAA AGTGCTGGGG TTACAGGCGT 360
GAGCCACTGC GCCCGGCCTC CTTGGTATTT TTATGTCTAT TTTTTTAGAT GGAGTCTCGC 420
TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC GATCAGCTCA CTGCAACCTC CACCTCGCGG 480
GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGAC GTCCATCAAC 540
ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGATAGGGTT TCACCATGTT GGCCAGGCTG 600
GTCTTGAACT GCCTACCTCA GGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 660
CAGGCGTAAG CCACCTGCGC CTGGCCGGTA TTTTTAAATT AGAGTTCTTC TAAGATTTAT 720
CTGAAAAAGT TACACTACTA AAAAATTTGC AACCCACACC CAAGGACATA ATTTGTCTGG 780
GCATAGAGAC TTGATGGCAC TTCAAGTAGC TGGATGAGCT TCTCTTAACA TGCGATTTCT 840
CTCAGGTTTA CATTCTTCTT GACTGCCCTT GTTCCTTTCC TATTCTATTT GAAGCAAAAT 900
GGTTAACGTT CTTCCACTTT CACCAGGACA GCCCTATTTG CCCCTTCCTT GTCCTTGTTA 960
GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG GTCGGAACAG TTAATAGCAT TGGGGATTGT 1020
CGCTTGTTCC CTGTAGATGA AAAGTATTTT TCTATTGTTT AAAAAAAAAT CGAGGTCATT 1080
CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG GGAGGAAGTC ATGGGCATGA GGATGAGTCA 1140
TCAGGCAGCA GCACGAGGCT GCAGGCGTGA GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG 1200
GCTTGGATCC CTGAGCGGAG CAGGCCACTG GGGCCTTCTG CCGTGAGAAG AGACCTACTG 1260
AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG CTTCTGACCT GTAGGACAGT GGTCAGCGTG 1320
GGCGGGTGGA GGCACAGGAG AAGGCCGACA GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT 1380
GGAAAATGAA GTTCAGAGTT GTTTGGACTG TCTGAAGTAG GATAGAACCA GCCTTAGCCC 1440
TAGTTAGGTA ACACATGGCA GAGGCACCTG AGCAAAGACG TGAGCTGGAC CATGGGCTTC 1500
CTGGCAGGAC TTCCACGGAG GAGGGCGAGG GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT 1560
GCCGTCCACG AAGCCTCCTG AGGCCCCAGA TGAGTCACCA GACAACAGCC TGTCTACTTA 1620
AAGCAACTGC TGGGCAACTG CTGAGTAGAA CAGTCCCTAA CCACATGAAC ACTGGGGAGG 1680
AGGTTCTGAA AGACGCTGCT GGGTGCAAGG TCCCTAACTA GGGTAATCCA ATTTCACTCC 1740
AGGCTAACAT GAGAAATTAT GACTCCAGCA GCCAATCCTG TGGGCCGTGA GAGAGTGGGA 1800
GAGGGATTTT CCAGATATAA GTCCCACTAG AGCTTCTTTT TTTTTTTTTT TTTTGATACG 1860
GAGTCTCACT CTGTTATCCA CGCTGGAGTG CAGTGGCACC ATCTCGGCTC ACTGCAAGCT 1920
CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC CCCAGCCTCC TGAGCAGATG GGACTACAGA 1980
TGTGCACCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA GAGACAGGGT TTCACTATGT 2040
CGGCCAGGCT GGTCTCGAAC TCCTGACCTC ATGATTCTCC TGCCTTGGCC TCCTAAAGTG 2100
TTGGGATCAC TGGCATAAGC CACAGCTTCC GGCTGAGTCC CACTAGAGCT TCTAAGAAGA 2160
AATTAGGGAA GCAGGATTAT GAGAGGCCTG GTCCCACTCA CAGTGTGCGA CATCACTGAT 2220
GACTATGCTT GGTTACCTGC CTTGTTATTT GCTACCTTTG TTATTGTCTA TTTCTTGGTA 2280
ATTAGTAGTA CACTATAGTG ATTAGGAGTG ATCAAGAAGA TGCCTGGCTT CATATTCCAA 2340
CTTTGTCGTT TACTAACTGT GAACTTGGCC GAGTTTTTTT TTTTTTGCTT GTTTGTTTTG 2400
TTTTGAGACA GGATCTCTCT CTGTCACCCA GGCTGGAGTG CAGTGGCGTG ATCTCAGCTC 2460
ACTGCAACCT CCACCTCCTG GAATCAAGGG ATCCTCCCAC CTTAGCCTCC CAAGTAGCTG 2520
AGATACACGT GTGCACCATC ACACCTGGCT AATTTTTGTA TTTTTTGTAG AGATGGTGTT 2580
TCACCATGTT GCCCAGGCTG GTCTTGAAGC CCTGGGCTCA AGCCATCACC CACCTTGGCC 2640
TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCTCCTGA CCTCAGGTGA TCCACCTGCC 2700
TCAGCCTCCC AAAGTGTTGG GATTACAGGC ATGAGCCACT GTGGCCAGTC CAGTTTCAAT 2760
TTCTTTATTT GTAAATTTGT AATAATGACA 2790